Allele Registry

Canonical Allele Identifier: PA168726

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV000131766

RCV000706879

RCV001030463

ClinVar Variation:

142568

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Leu1170Val	CA168724 NM_032043.3:c.3508C>G