Canonical Allele Identifier: PA2827936632
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2664368

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ile189Val
CA4239602
NM_001354800.1:c.565A>G