Canonical Allele Identifier: PA2580490784
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1746350
ClinVar RCV Id: RCV002340943 RCV003883198
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Gly176Glu
CA367401680
NM_033507.3:c.527G>A