Canonical Allele Identifier: PA2829391881
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 825447
ClinVar RCV Id: RCV001023547 RCV001301354
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Phe17Cys
CA400336669
NM_002876.4:c.50T>G