Allele Registry

Canonical Allele Identifier: PA166322

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV000130394

RCV000200420

RCV000590600

RCV000662423

RCV001290444

RCV003315892

RCV004532557

ClinVar Variation:

141761

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Pro210Ser	CA166320 NM_032043.3:c.628C>T