Canonical Allele Identifier: PA2830123896
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36185

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Arg391Leu
CA213733
NM_033508.3:c.1172G>T