Allele Registry

Canonical Allele Identifier: PA188886

Gene: RAD51C HGNC NCBI

ClinVar RCV:

RCV000163662

RCV000228544

RCV000479892

RCV001188570

RCV001195006

RCV003617911

ClinVar Variation:

184411

926172

HGVS (amino-acid)	Matching Registered Transcripts
NP_478123.1:p.Gly3Arg	CA188884 NM_058216.3:c.7G>A CA400336093 NM_058216.3:c.7G>C CA3057228037 NM_058216.3:c.6_7delinsGC