Canonical Allele Identifier: PA213829
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36244

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Val226Ala
CA213828
NM_000162.5:c.677T>C