Allele Registry

Canonical Allele Identifier: PA2827937098

Gene: GCK HGNC NCBI

ClinVar Variation Id: 129140

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341730.1:p.Cys34Phe	CA152950 NM_001354801.1:c.101G>T