Canonical Allele Identifier: PA2741997128
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 2738799
ClinVar RCV Id: RCV003508932
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Leu220Pro
CA400349774
NM_058216.3:c.659T>C