Canonical Allele Identifier: PA2499295140
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1191898

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Thr207Met
CA367401337
NM_033507.3:c.620C>T