Canonical Allele Identifier: PA658820286
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 538772
ClinVar RCV Id: RCV000648236
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Leu134Ser
CA400342097
NM_058216.3:c.401T>C