Canonical Allele Identifier: PA2829447736
Gene: UNG HGNC NCBI

Linked Data

ClinVar Variation Id: 440391

Amino-acid Alleles

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