Canonical Allele Identifier: PA913202214
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 630837
ClinVar RCV Id: RCV001238382 RCV000776843 RCV003461042
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Thr200Ala
CA400349233
NM_058216.3:c.598A>G