Canonical Allele Identifier: PA2579975310
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 908615

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Thr342Pro
CA157913750
NM_000162.5:c.1024A>C