Canonical Allele Identifier: PA2579975618
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2574157
ClinVar RCV Id: RCV003318522

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Thr168Ala
CA367401753
NM_000162.5:c.502A>G