Allele Registry

Canonical Allele Identifier: PA288590

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV000116155

RCV000204181

RCV000214821

RCV000409119

RCV000410336

RCV001194197

RCV001354313

RCV003315658

ClinVar Variation:

128186

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Glu1111Gln	CA288588 NM_032043.3:c.3331G>C