Canonical Allele Identifier: PA2830123758
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36172

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Ile347Phe
CA213707
NM_033508.3:c.1039A>T