Canonical Allele Identifier: PA916039367
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804842

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Arg67Pro
CA367396939
NM_001354802.1:c.200G>C