Canonical Allele Identifier: PA2829392086
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 1773963
ClinVar RCV Id: RCV002389880
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Val50Ala
CA400339518
NM_002876.4:c.149T>C