Canonical Allele Identifier: PA2579978702
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2700200
ClinVar RCV Id: RCV003547122

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ile159Thr
CA367401855
NM_000162.5:c.476T>C