Canonical Allele Identifier: PA2579980867
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2691835

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Cys220Phe
CA367401193
NM_000162.5:c.659G>T