Canonical Allele Identifier: PA2827936987
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2734991

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Arg397Cys
CA4239418
NM_001354800.1:c.1189C>T