Canonical Allele Identifier: PA645460358
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36172

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Ile349Phe
CA213707
NM_033507.3:c.1045A>T