Canonical Allele Identifier: PA2827936511
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 435307

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Leu122Ile
CA367402232
NM_001354800.1:c.364C>A