Canonical Allele Identifier: PA2579980309
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1338598

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Glu279Lys
CA157915593
NM_000162.5:c.835G>A