Canonical Allele Identifier: PA2830123609
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447422

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Val276Gly
CA367400467
NM_033508.3:c.827T>G