Canonical Allele Identifier: PA213791
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36223

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Arg155Gly
CA213790
NM_000162.5:c.463A>G