Canonical Allele Identifier: PA916039399
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36183

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Ile68Asn
CA213729
NM_001354803.2:c.203T>A