Canonical Allele Identifier: PA2579975561
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447413

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Thr228Ala
CA367400790
NM_000162.5:c.682A>G