Canonical Allele Identifier: PA2827936799
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 994611
ClinVar RCV Id: RCV001288182

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Asp274Glu
CA367400481
NM_001354800.1:c.822C>G
CA367400482
NM_001354800.1:c.822C>A