Canonical Allele Identifier: PA658669129
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447380

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Val375Met
CA367398877
NM_033507.3:c.1123G>A