Canonical Allele Identifier: PA213821
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36239

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Cys220Arg
CA213820
NM_000162.5:c.658T>C