Canonical Allele Identifier: PA2827936801
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2664365

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Arg275Gly
CA367400479
NM_001354800.1:c.823C>G