Canonical Allele Identifier: PA2827936914
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 129140

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Cys371Phe
CA152950
NM_001354800.1:c.1112G>T