Canonical Allele Identifier: PA645460749
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36176

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Arg378His
CA213715
NM_033507.3:c.1133G>A