Canonical Allele Identifier: PA2825042344
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1210150

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Cys129Tyr
CA367402156
NM_000162.5:c.386G>A