Canonical Allele Identifier: PA2827937441
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585916

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Val133Glu
CA4239373
NM_001354803.2:c.398T>A