Canonical Allele Identifier: PA2829391809
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 1716841
ClinVar RCV Id: RCV002296066
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Thr5Ala
CA400336151
NM_002876.4:c.13A>G