Allele Registry

Canonical Allele Identifier: PA299928

Gene: RAD51D HGNC NCBI

ClinVar RCV:

RCV000160945

RCV000227224

RCV000586341

RCV000709444

RCV001354078

RCV001420703

RCV001798559

ClinVar Variation:

182856

HGVS (amino-acid)	Matching Registered Transcripts
NP_002869.3:p.Cys119Arg	CA299926 NM_002878.4:c.355T>C