Canonical Allele Identifier: PA2579979540
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804856

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Gly246Ala
CA367400661
NM_000162.5:c.737G>C