Canonical Allele Identifier: PA2579982895
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 435311

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Arg250His
CA4239531
NM_000162.5:c.749G>A