Canonical Allele Identifier: PA096418
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804852

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Met210Thr
CA367401300
NM_000162.5:c.629T>C