Canonical Allele Identifier: PA2827936609
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 976272

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Glu177Leu
CA1139660058
NM_001354800.1:c.529_530delinsTT