Allele Registry

Canonical Allele Identifier: PA192212

Gene: RAD51C HGNC NCBI

ClinVar RCV:

RCV000164977

RCV000409780

RCV000411003

RCV000484927

ClinVar Variation:

185535

HGVS (amino-acid)	Matching Registered Transcripts
NP_478123.1:p.Leu39Val	CA192210 NM_058216.3:c.115C>G CA3057228841 NM_058216.3:c.114_115delinsAG