Canonical Allele Identifier: PA2829447736
Gene: UNG HGNC NCBI

Linked Data

ClinVar Variation Id: 440391
ClinVar RCV Id: RCV000506946 RCV000687269
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003353.1:p.Arg79Cys
CA6772541
NM_003362.4:c.235C>T