Canonical Allele Identifier: PA2830123455
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2136518

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Gly226Ser
CA367401117
NM_033508.3:c.676G>A