Allele Registry

Canonical Allele Identifier: PA645433727

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV000216569

RCV000219246

RCV000460900

RCV000662901

RCV001194199

RCV003316230

ClinVar Variation:

233799

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.His587Leu	CA10577562 NM_032043.3:c.1760A>T