Canonical Allele Identifier: PA2827936979
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1522625

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Arg394Leu
CA367398578
NM_001354800.1:c.1181G>T