Canonical Allele Identifier: PA2827936996
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1807287
ClinVar RCV Id: RCV002475244

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Gly407Asp
CA367398350
NM_001354800.1:c.1220G>A