Canonical Allele Identifier: PA2830122286
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2734991

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Arg398Cys
CA4239418
NM_033507.3:c.1192C>T