Canonical Allele Identifier: PA2827936938
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1098819

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.His380Pro
CA367398780
NM_001354800.1:c.1139A>C