appears_in: []
depends_on: []
deprecated: false
description: ClinVar archives reports of relationships among medically important variants
  and phenotypes. It records human variation, interpretations of the relationship
  specific variations to human health, and supporting evidence for each interpretation.
  Each ClinVar record (RCV identifier) represents an aggregated view of interpretations
  of  the same variation and condition from one or more submitters. Submissions for
  individual variation/phenotype combinations (SCV identifier) are also collected
  and made available separately. This collection references the Record Report, based
  on RCV accession.
example: RCV000033555.3
homepage: http://www.ncbi.nlm.nih.gov/clinvar/
keywords: []
mappings:
  biocontext: CLINVAR.RECORD
  miriam: clinvar.record
  n2t: clinvar.record
name: ClinVar Record
namespace_in_lui: false
part_of: clinvar
pattern: ^RCV\d+(\.\d+)?$
preferred_prefix: clinvar.record
prefix: clinvar.record
providers: []
publications: []
synonyms: []
uri_format: http://www.ncbi.nlm.nih.gov/clinvar/$1
