Canonical Allele Identifier: PA1139760359
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 945078
ClinVar RCV Id: RCV001215619
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Ala139Pro
CA400343808
NM_058216.3:c.415G>C