Canonical Allele Identifier: PA2830123206
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2574157
ClinVar RCV Id: RCV003318522

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Thr167Ala
CA367401753
NM_033508.3:c.499A>G