Canonical Allele Identifier: PA2830123232
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1746353

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Gly174Val
CA367401683
NM_033508.3:c.521G>T