Canonical Allele Identifier: PA2827936510
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2735019

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Leu122Pro
CA367402227
NM_001354800.1:c.365T>C