Canonical Allele Identifier: PA2579980555
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 976272

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Glu177Leu
CA1139660058
NM_000162.5:c.529_530delinsTT