Allele Registry

Canonical Allele Identifier: PA645432811

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV000483934

RCV000565081

RCV000811860

ClinVar Variation:

422627

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Pro163Ser	CA16620544 NM_032043.3:c.487C>T