Canonical Allele Identifier: PA658671097
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 486278
ClinVar RCV Id: RCV000564406
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Gln137Pro
CA400343722
NM_058216.3:c.410A>C