Canonical Allele Identifier: PA2827936593
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2574157
ClinVar RCV Id: RCV003318522

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Thr168Ala
CA367401753
NM_001354800.1:c.502A>G