Canonical Allele Identifier: PA2827937003
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1801514
ClinVar RCV Id: RCV002463834

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Gly410Val
CA367398308
NM_001354800.1:c.1229G>T