Canonical Allele Identifier: PA2741997085
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 2847263
ClinVar RCV Id: RCV003617402
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Leu201Phe
CA400349250
NM_058216.3:c.601C>T