Canonical Allele Identifier: PA2827937232
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804842

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Arg110Pro
CA367396939
NM_001354801.1:c.329G>C