Canonical Allele Identifier: PA2827937161
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1301416

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Arg55Gly
CA367398625
NM_001354801.1:c.163C>G