Canonical Allele Identifier: PA2830123311
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447409

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Met196Thr
CA367401431
NM_033508.3:c.587T>C