Canonical Allele Identifier: PA2827937297
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 995102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Arg17His
CA367398533
NM_001354802.1:c.50G>A