Canonical Allele Identifier: PA2830123460
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447413

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Thr227Ala
CA367400790
NM_033508.3:c.679A>G