Canonical Allele Identifier: PA2829392018
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 2447777
ClinVar RCV Id: RCV003176623
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Leu39Pro
CA400337535
NM_002876.4:c.116T>C