Canonical Allele Identifier: PA658669149
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447386

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Gly411Asp
CA367398309
NM_033507.3:c.1232G>A