Canonical Allele Identifier: PA206280
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 211075

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Asp262Asn
CA206279
NM_000162.5:c.784G>A