Canonical Allele Identifier: PA2830124065
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2664359

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Gly443Asp
CA367396980
NM_033508.3:c.1328G>A