Canonical Allele Identifier: PA299889
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 182836
ClinVar RCV Id: RCV000160924 RCV000563267 RCV000807077 RCV000781796 RCV001310207
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Arg312Trp
CA299887
NM_058216.3:c.934C>T