Canonical Allele Identifier: PA096477
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 16134

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Thr228Met
CA260620
NM_000162.5:c.683C>T