Canonical Allele Identifier: PA645509947
Gene: UNG HGNC NCBI

Linked Data

ClinVar Variation Id: 440391
ClinVar RCV Id: RCV000506946 RCV000687269
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_550433.1:p.Arg88Cys
CA6772541
NM_080911.3:c.262C>T