Canonical Allele Identifier: PA2827936540
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 451690

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Lys143Leu
CA658655971
NM_001354800.1:c.427_428delinsCT