Canonical Allele Identifier: PA2827937260
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1256304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Cys2Tyr
CA367398751
NM_001354802.1:c.5G>A