Allele Registry

Canonical Allele Identifier: PA169465

Gene: BRIP1 HGNC NCBI

ClinVar Allele:

152523

ClinVar RCV:

RCV000132232

RCV000213770

RCV000687515

RCV000990039

RCV002267884

RCV004532579

ClinVar Variation:

142809

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Asn109Ser	CA169463 NM_032043.3:c.326A>G