Allele Registry

Canonical Allele Identifier: PA168514

Gene: BRIP1 HGNC NCBI

ClinVar Allele:

152206

ClinVar RCV:

RCV000131634

RCV000231093

RCV000662676

RCV001174711

RCV001559562

RCV003315913

ClinVar Variation:

142492

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Arg162Leu	CA168512 NM_032043.3:c.485G>T