Canonical Allele Identifier: PA2830123464
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 16134

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Thr227Met
CA260620
NM_033508.3:c.680C>T