Allele Registry

Canonical Allele Identifier: PA165628

Gene: BRIP1 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

151213

ClinVar RCV:

RCV000130056

RCV000663220

RCV000699539

RCV001194712

RCV001255230

RCV002273958

RCV003460909

ClinVar Variation:

141499

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Arg848His	CA165626 NM_032043.3:c.2543G>A