Canonical Allele Identifier: PA2829391928
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 2820189
ClinVar RCV Id: RCV003618528
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Val23Ala
CA400336863
NM_002876.4:c.68T>C