Canonical Allele Identifier: PA2580498160
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 1719318
ClinVar RCV Id: RCV002302078
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Leu201Arg
CA400349255
NM_058216.3:c.602T>G