Canonical Allele Identifier: PA213807
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36231
ClinVar RCV Id: RCV000029894 RCV002463601
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Glu196Gly
CA213806
NM_000162.5:c.587A>G