Canonical Allele Identifier: PA1139735312
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 872751

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Arg55Leu
CA367398811
NM_001354803.2:c.164G>T