Canonical Allele Identifier: PA2827936954
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2136509

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ala384Glu
CA367398725
NM_001354800.1:c.1151C>A