Allele Registry

Canonical Allele Identifier: PA169870

Gene: RAD51D HGNC NCBI

ClinVar RCV:

RCV000132446

RCV000476134

RCV003477563

ClinVar Variation:

142955

HGVS (amino-acid)	Matching Registered Transcripts
NP_002869.3:p.Gly112Asp	CA169868 NM_002878.4:c.335G>A