Allele Registry

Canonical Allele Identifier: PA2499292741

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV001597648

ClinVar Variation:

1221357

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Ser919Thr	CA400481599 NM_032043.3:c.2755T>A