Canonical Allele Identifier: PA645459522
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36223

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Arg156Gly
CA213790
NM_033507.3:c.466A>G