Canonical Allele Identifier: PA2579981433
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 994611
ClinVar RCV Id: RCV001288182

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Asp274Glu
CA367400481
NM_000162.5:c.822C>G
CA367400482
NM_000162.5:c.822C>A