Canonical Allele Identifier: PA2579980814
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1807288
ClinVar RCV Id: RCV002475245

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Glu237Val
CA367400727
NM_000162.5:c.710A>T