Canonical Allele Identifier: PA2830122199
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804836

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Ala385Val
CA367398721
NM_033507.3:c.1154C>T