Canonical Allele Identifier: PA916050245
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804851

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Thr210Met
CA367401309
NM_033507.3:c.629C>T