Canonical Allele Identifier: PA2829391907
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 538775
ClinVar RCV Id: RCV000648243 RCV002358853
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Ser20Phe
CA400336751
NM_002876.4:c.59C>T