Canonical Allele Identifier: PA2827937028
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36189

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Phe423Tyr
CA213740
NM_001354800.1:c.1268T>A