Canonical Allele Identifier: PA2827936665
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804344

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ala208Thr
CA367401322
NM_001354800.1:c.622G>A