Canonical Allele Identifier: PA916039357
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804837

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Leu6Val
CA367398705
NM_001354802.1:c.16C>G