Canonical Allele Identifier: PA2830122101
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 872751

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Arg378Leu
CA367398811
NM_033507.3:c.1133G>T