Canonical Allele Identifier: PA2830122278
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 995102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Arg398His
CA367398533
NM_033507.3:c.1193G>A