Canonical Allele Identifier: PA2830122218
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804837

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Leu387Val
CA367398705
NM_033507.3:c.1159C>G