Canonical Allele Identifier: PA213730
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36183

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ile390Asn
CA213729
NM_000162.5:c.1169T>A