Canonical Allele Identifier: PA2827937363
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804832

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Leu33Pro
CA367399180
NM_001354803.2:c.98T>C