Canonical Allele Identifier: PA2499295673
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 1055129
ClinVar RCV Id: RCV001363744
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Arg212Leu
CA400349505
NM_058216.3:c.635G>T