Canonical Allele Identifier: PA2829392251
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 492366
ClinVar RCV Id: RCV000584649 RCV001798906 RCV001853939 RCV003321690
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.His82Tyr
CA400340328
NM_002876.4:c.244C>T