Canonical Allele Identifier: PA2830123425
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36239

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Cys219Arg
CA213820
NM_033508.3:c.655T>C