Canonical Allele Identifier: PA2827937139
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1734018
ClinVar RCV Id: RCV002348865

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Ala47Thr
CA367398732
NM_001354801.1:c.139G>A