Canonical Allele Identifier: PA2579980880
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2136521
ClinVar RCV Id: RCV003060106

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Cys213Tyr
CA367401270
NM_000162.5:c.638G>A