Allele Registry

Canonical Allele Identifier: PA298830

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV000160320

RCV000167936

RCV000212300

RCV000662866

RCV002298487

RCV003315952

ClinVar Variation:

182331

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Thr132Ser	CA298828 NM_032043.3:c.394A>T CA400484585 NM_032043.3:c.395C>G