Canonical Allele Identifier: PA2827936690
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36239

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Cys220Arg
CA213820
NM_001354800.1:c.658T>C