Canonical Allele Identifier: PA645371757
Gene: OGT HGNC NCBI

Linked Data

ClinVar Variation Id: 428571
ClinVar RCV Id: RCV000492048

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_858059.1:p.Arg274Pro
CA413546092
NM_181673.3:c.821G>C