Canonical Allele Identifier: PA2827936918
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447380

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Val374Met
CA367398877
NM_001354800.1:c.1120G>A