Canonical Allele Identifier: PA2827936418
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 393453

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Arg43His
CA4239718
NM_001354800.1:c.128G>A