Canonical Allele Identifier: PA2829391775
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 1692063
ClinVar RCV Id: RCV002259186
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Arg2Cys
CA8677116
NM_002876.4:c.4C>T