Canonical Allele Identifier: PA2573296716
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 1522818
ClinVar RCV Id: RCV002048769
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Cys213Ser
CA400349512
NM_058216.3:c.637T>A
CA400349526
NM_058216.3:c.638G>C