Canonical Allele Identifier: PA2579979062
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2136531
ClinVar RCV Id: RCV003037224

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ile19Asn
CA367403826
NM_000162.5:c.56T>A