Canonical Allele Identifier: PA2827936836
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 16136

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Gly299Arg
CA126212
NM_001354800.1:c.895G>C