Canonical Allele Identifier: PA645391056
Gene: OGT HGNC NCBI

Linked Data

ClinVar Variation Id: 428570
ClinVar RCV Id: RCV000492058
ClinVar Variation Id: 804282
ClinVar RCV Id: RCV000991239

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_858058.1:p.Leu254Phe
CA413545253
NM_181672.3:c.762G>C
CA413545259
NM_181672.3:c.762G>T