Canonical Allele Identifier: PA2827936956
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 982610

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Gly385Glu
CA367398712
NM_001354800.1:c.1154G>A