Allele Registry

Canonical Allele Identifier: PA2580472166

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV002460200

ClinVar Variation:

1731524

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Ala1150Ser	CA400478703 NM_032043.3:c.3448G>T