Allele Registry

Canonical Allele Identifier: PA645435478

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV000222623

RCV000458509

RCV000481975

RCV001798718

ClinVar Variation:

232249

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