Allele Registry

Canonical Allele Identifier: PA190977

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV000164448

RCV000586440

RCV000699974

ClinVar Variation:

185088

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Thr908Ile	CA190975 NM_032043.3:c.2723C>T