Canonical Allele Identifier: PA2829391778
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 548876
ClinVar RCV Id: RCV000663126 RCV000772906 RCV000986010 RCV001861727 RCV003316791
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Arg2Gly
CA400336071
NM_002876.4:c.4C>G