Allele Registry

Canonical Allele Identifier: PA163645

Gene: BRIP1 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000129008

RCV000410906

RCV000412441

RCV000590794

RCV001081667

RCV001355322

RCV001800423

RCV003149886

RCV003315867

RCV004532542

ClinVar Variation:

140819

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Arg1035Cys	CA163643 NM_032043.3:c.3103C>T