Canonical Allele Identifier: PA2830121986
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 908615

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Thr343Pro
CA157913750
NM_033507.3:c.1027A>C