Allele Registry

Canonical Allele Identifier: PA299889

Gene: RAD51C HGNC NCBI

ClinVar Allele:

180920

ClinVar RCV:

RCV000160924

RCV000563267

RCV000781796

RCV000807077

RCV001310207

ClinVar Variation:

182836

HGVS (amino-acid)	Matching Registered Transcripts
NP_478123.1:p.Arg312Trp	CA299887 NM_058216.3:c.934C>T