Canonical Allele Identifier: PA645460348
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 229887
ClinVar RCV Id: RCV000222506 RCV000505229 RCV001753654 RCV002290965
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Arg312Gln
CA8677363
NM_058216.3:c.935G>A