Allele Registry

Canonical Allele Identifier: PA658663677

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV000540935

RCV002431577

ClinVar Variation:

461126

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Asn905Ser	CA400481678 NM_032043.3:c.2714A>G