Canonical Allele Identifier: PA891855369
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585916

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Val456Glu
CA4239373
NM_033507.3:c.1367T>A