Canonical Allele Identifier: PA2742024921
Gene: OGT HGNC NCBI

Linked Data

ClinVar Variation Id: 2759272
ClinVar RCV Id: RCV003564659
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_858059.1:p.Asn7His
CA413532789
NM_181673.3:c.19A>C