Canonical Allele Identifier: PA2579974559
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 435309

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Val33Glu
CA367403606
NM_000162.5:c.98T>A