Canonical Allele Identifier: PA2741997429
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2735019

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Leu123Pro
CA367402227
NM_033507.3:c.368T>C