Allele Registry

Canonical Allele Identifier: PA288569

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV000116148

RCV000212329

RCV000229209

RCV000410789

RCV000412341

RCV000656814

RCV003315654

ClinVar Variation:

128179

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Ile902Met	CA288567 NM_032043.3:c.2706A>G