Canonical Allele Identifier: PA2830123869
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804836

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Ala383Val
CA367398721
NM_033508.3:c.1148C>T