Canonical Allele Identifier: PA2829391906
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 1366390
ClinVar RCV Id: RCV001944656
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Ser20Tyr
CA400336749
NM_002876.4:c.59C>A