Canonical Allele Identifier: PA2827936890
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 908615

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Thr342Pro
CA157913750
NM_001354800.1:c.1024A>C