Canonical Allele Identifier: PA2827937360
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 987827

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Arg23Gly
CA367399354
NM_001354803.2:c.67C>G