Canonical Allele Identifier: PA2579975453
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3230479
ClinVar RCV Id: RCV004520630

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Tyr273Cys
CA367400492
NM_000162.5:c.818A>G