Canonical Allele Identifier: PA2827936953
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1734018
ClinVar RCV Id: RCV002348865

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ala384Thr
CA367398732
NM_001354800.1:c.1150G>A