Canonical Allele Identifier: PA2827937284
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1301416

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Arg12Gly
CA367398625
NM_001354802.1:c.34C>G