Canonical Allele Identifier: PA2580229378
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1700674

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.His94Arg
CA367398216
NM_001354803.2:c.281A>G