Canonical Allele Identifier: PA2827936927
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585908

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Arg377Cys
CA367398826
NM_001354800.1:c.1129C>T