Canonical Allele Identifier: PA2830122413
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1800884

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Arg423Leu
CA157911892
NM_033507.3:c.1268G>T