Canonical Allele Identifier: PA2827936985
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 995102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Arg397His
CA367398533
NM_001354800.1:c.1190G>A