Allele Registry

Canonical Allele Identifier: PA287995

Gene: RAD51D HGNC NCBI

ClinVar RCV:

RCV000115822

RCV000233793

RCV000656967

RCV000709427

RCV001354391

RCV001818279

RCV003149804

RCV003492497

ClinVar Variation:

127896

HGVS (amino-acid)	Matching Registered Transcripts
NP_002869.3:p.Ile311Asn	CA287993 NM_002878.4:c.932T>A