Allele Registry

Canonical Allele Identifier: PA658724442

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV000581888

RCV000636141

RCV000989981

ClinVar Variation:

491464

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Pro1092Gln	CA400479077 NM_032043.3:c.3275C>A