Canonical Allele Identifier: PA2829391923
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 2692721
ClinVar RCV Id: RCV003507522
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Ala22Gly
CA400336837
NM_002876.4:c.65C>G