Allele Registry

Canonical Allele Identifier: PA191783

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV000164796

RCV000217145

RCV000457977

RCV000999642

RCV003493473

ClinVar Variation:

185386

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Ile633Leu	CA191781 NM_032043.3:c.1897A>C