Canonical Allele Identifier: PA2829391827
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 478608
ClinVar RCV Id: RCV000559705 RCV000582971
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Arg7Cys
CA400336236
NM_002876.4:c.19C>T