Canonical Allele Identifier: PA096238
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 211076

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Glu279Gln
CA208420
NM_000162.5:c.835G>C