Allele Registry

Canonical Allele Identifier: PA197071

Gene: RAD51D HGNC NCBI

ClinVar RCV:

RCV000166932

RCV001326333

ClinVar Variation:

187224

HGVS (amino-acid)	Matching Registered Transcripts
NP_002869.3:p.Ser62Trp	CA197069 NM_002878.4:c.185C>G