Canonical Allele Identifier: PA2827936651
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36233

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Met202Thr
CA213810
NM_001354800.1:c.605T>C