Canonical Allele Identifier: PA2830123955
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447386

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Gly409Asp
CA367398309
NM_033508.3:c.1226G>A