Canonical Allele Identifier: PA299866
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 182828
ClinVar RCV Id: RCV000160916 RCV000168412 RCV000234871 RCV000663073 RCV000781789 RCV001257495
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Arg249His
CA299864
NM_058216.3:c.746G>A