Allele Registry

Canonical Allele Identifier: PA2829447915

Gene: UNG HGNC NCBI

ClinVar RCV:

RCV000013086

ClinVar Variation:

12292

HGVS (amino-acid)	Matching Registered Transcripts
NP_003353.1:p.Phe242Ser	CA122119 NM_003362.4:c.725T>C