Canonical Allele Identifier: PA2827936711
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 16134

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Thr228Met
CA260620
NM_001354800.1:c.683C>T