Canonical Allele Identifier: PA2825042500
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 995102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Arg397His
CA367398533
NM_000162.5:c.1190G>A