Canonical Allele Identifier: PA213835
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36248

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Met235Thr
CA213834
NM_000162.5:c.704T>C