Canonical Allele Identifier: PA2830122478
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1338523
ClinVar RCV Id: RCV001817894

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Glu441Gly
CA367397030
NM_033507.3:c.1322A>G