Canonical Allele Identifier: PA213726
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36181

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ala387Glu
CA213725
NM_000162.5:c.1160C>A