Canonical Allele Identifier: PA2830123282
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 431972

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Ile188Thr
CA367401550
NM_033508.3:c.563T>C