Canonical Allele Identifier: PA2580490812
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2136518

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Gly228Ser
CA367401117
NM_033507.3:c.682G>A