Canonical Allele Identifier: PA2829391911
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 1750402
ClinVar RCV Id: RCV002355706
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Ser20Ala
CA400336746
NM_002876.4:c.58T>G