Allele Registry

Canonical Allele Identifier: PA167443

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV000130948

RCV000367894

RCV000464105

RCV001192822

RCV002254681

RCV004532567

ClinVar Variation:

142113

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Asn955His	CA167441 NM_032043.3:c.2863A>C