Canonical Allele Identifier: PA2827937361
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36172

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Ile26Phe
CA213707
NM_001354803.2:c.76A>T