Canonical Allele Identifier: PA2579982034
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1301416

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Arg392Gly
CA367398625
NM_000162.5:c.1174C>G