Canonical Allele Identifier: PA2579978411
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2735019

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Leu122Pro
CA367402227
NM_000162.5:c.365T>C