Allele Registry

Canonical Allele Identifier: PA915979435

Gene: RAD51D HGNC NCBI

ClinVar RCV:

RCV000569593

RCV001316887

ClinVar Variation:

484786

HGVS (amino-acid)	Matching Registered Transcripts
NP_001136043.1:p.Arg252Gly	CA399087669 NM_001142571.2:c.754C>G