Allele Registry

Canonical Allele Identifier: PA298856

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV000160330

RCV000216538

RCV001065714

ClinVar Variation:

182340

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Pro47Thr	CA298854 NM_032043.3:c.139C>A