Canonical Allele Identifier: PA2829392405
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 1729179
ClinVar RCV Id: RCV002324728
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Asp108Tyr
CA400341215
NM_002876.4:c.322G>T