Canonical Allele Identifier: PA916039354
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36194

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Leu93Pro
CA213749
NM_001354801.1:c.278T>C