Allele Registry

Canonical Allele Identifier: PA193146

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV000165345

RCV000206065

RCV000219928

RCV000662796

RCV001781512

RCV002225482

RCV003316042

ClinVar Variation:

185848

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Arg251Cys	CA193144 NM_032043.3:c.751C>T