Canonical Allele Identifier: PA2827936990
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36187

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Arg403Gly
CA213737
NM_001354800.1:c.1207C>G