Canonical Allele Identifier: PA2827937254
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2578350
ClinVar RCV Id: RCV003326076

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Gln128_Ter129insTrpGluGlnTrpProGlnAlaGlnGlyGlyCysHisSerProThrAlaProArgLeuHisGlyGluValLeuProThrArgAlaArgSerLeuAlaGlyGlnGluAlaTrpProCysGlnAspProGlyArgLeuProTyrArgTrpGlyThrGluArgAlaSerSerLeuSerPheSerValGlyGlnProGlnGlyProAsnGlyGlyAlaAlaGlyAlaGlyThrGluThrLeuGluAlaProHisLeuSerArgTrpAsnGlnPheProArgArgGluLeuLeuThrGlnAspPheAspAlaPheProHisCysGlnSerCysTrpProArgLeuGlyProGlySerGlyLysGlyCysProLeuAspProAlaValAlaSerLeuProTrpGluLeuIleLeuCysGlyGluAlaAlaProThrAla
CA367396716
NM_001354801.1:c.387A>G