Canonical Allele Identifier: PA341590
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 21078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Gly264Ser
CA341589
NM_000162.5:c.790G>A