Canonical Allele Identifier: PA2579978901
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1801514
ClinVar RCV Id: RCV002463834

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Gly410Val
CA367398308
NM_000162.5:c.1229G>T