Canonical Allele Identifier: PA096310
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 16136

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Gly299Arg
CA126212
NM_000162.5:c.895G>C