Canonical Allele Identifier: PA213797
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36226
ClinVar RCV Id: RCV000029889 RCV002463598
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ala176Gly
CA213796
NM_000162.5:c.527C>G