Canonical Allele Identifier: PA645435478
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 232249
ClinVar RCV Id: RCV000222623 RCV000481975 RCV000458509 RCV001798718
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ile896Val
CA8690466
NM_032043.3:c.2686A>G