Canonical Allele Identifier: PA658669022
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447413

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Thr229Ala
CA367400790
NM_033507.3:c.685A>G