Canonical Allele Identifier: PA2827937313
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447386

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Gly30Asp
CA367398309
NM_001354802.1:c.89G>A