Allele Registry

Canonical Allele Identifier: PA157703

Gene: BRIP1 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000120399

RCV000131535

RCV000588835

RCV000662392

RCV000709540

RCV001030535

RCV001083712

RCV001356698

RCV003315736

RCV003492524

ClinVar Variation:

133755

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Arg814Cys	CA157701 NM_032043.3:c.2440C>T