Allele Registry

Canonical Allele Identifier: PA658817222

Gene: BRIP1 HGNC NCBI

ClinVar Allele:

506619

ClinVar RCV:

RCV000606452

RCV001860262

ClinVar Variation:

506573

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Ser1237Tyr	CA400477772 NM_032043.3:c.3710C>A