Canonical Allele Identifier: PA213734
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36185

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Arg392Leu
CA213733
NM_000162.5:c.1175G>T