Canonical Allele Identifier: PA331907
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 128210
ClinVar RCV Id: RCV000116179 RCV000411451 RCV000585995 RCV000765378 RCV000206074 RCV000778506 RCV001356788 RCV001798365 RCV001195025 RCV001778711
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Leu262Val
CA331905
NM_058216.3:c.784T>G