Canonical Allele Identifier: PA2827936925
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 872751

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Arg377Leu
CA367398811
NM_001354800.1:c.1130G>T