Canonical Allele Identifier: PA2827936967
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36183

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ile390Asn
CA213729
NM_001354800.1:c.1169T>A