Canonical Allele Identifier: PA2579982466
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 393453

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Arg43His
CA4239718
NM_000162.5:c.128G>A