Canonical Allele Identifier: PA2830123475
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36247

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Ala231Thr
CA213832
NM_033508.3:c.691G>A