Canonical Allele Identifier: PA096149
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1734018
ClinVar RCV Id: RCV002348865

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ala384Thr
CA367398732
NM_000162.5:c.1150G>A