Allele Registry

Canonical Allele Identifier: PA096712

Gene: UNG HGNC NCBI

ClinVar RCV:

RCV000013086

ClinVar Variation:

12292

HGVS (amino-acid)	Matching Registered Transcripts
NP_550433.1:p.Phe251Ser	CA122119 NM_080911.3:c.752T>C