Canonical Allele Identifier: PA2827936393
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 435309

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Val33Glu
CA367403606
NM_001354800.1:c.98T>A