Canonical Allele Identifier: PA2830123436
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 435306

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Gly222Ser
CA367401165
NM_033508.3:c.664G>A