Allele Registry

Canonical Allele Identifier: PA190837

Gene: RAD51D HGNC NCBI

ClinVar RCV:

RCV000164390

RCV000236527

RCV000461972

RCV001798582

RCV002281979

ClinVar Variation:

185036

HGVS (amino-acid)	Matching Registered Transcripts
NP_002869.3:p.Ser62Leu	CA190835 NM_002878.4:c.185C>T