Canonical Allele Identifier: PA645461077
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36185

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Arg393Leu
CA213733
NM_033507.3:c.1178G>T