Canonical Allele Identifier: PA2830122324
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1801514
ClinVar RCV Id: RCV002463834

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Gly411Val
CA367398308
NM_033507.3:c.1232G>T