Canonical Allele Identifier: PA916039355
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36195

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Ile99Asn
CA213751
NM_001354801.1:c.296T>A