Canonical Allele Identifier: PA645460311
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 16136

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Gly300Arg
CA126212
NM_033507.3:c.898G>C