Canonical Allele Identifier: PA658668962
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447401

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Arg156Thr
CA367401902
NM_033507.3:c.467G>C