Canonical Allele Identifier: PA2827936578
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2700200
ClinVar RCV Id: RCV003547122

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ile159Thr
CA367401855
NM_001354800.1:c.476T>C