Canonical Allele Identifier: PA2580490697
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2136531
ClinVar RCV Id: RCV003037224

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Ile20Asn
CA367403826
NM_033507.3:c.59T>A