Canonical Allele Identifier: PA645371759
Gene: OGT HGNC NCBI

Linked Data

ClinVar Variation Id: 428571
ClinVar RCV Id: RCV000492048

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_858058.1:p.Arg284Pro
CA413546092
NM_181672.3:c.851G>C