Canonical Allele Identifier: PA2579979579
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2136520
ClinVar RCV Id: RCV003060105

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Gly223Val
CA367401157
NM_000162.5:c.668G>T