Canonical Allele Identifier: PA152956
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 129145

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Thr206Pro
CA152955
NM_000162.5:c.616A>C