Canonical Allele Identifier: PA645460058
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 409837
ClinVar RCV Id: RCV000574346 RCV000464422 RCV000485483 RCV001526803
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Arg12Trp
CA8677126
NM_058216.3:c.34C>T