Canonical Allele Identifier: PA2827937266
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3024419
ClinVar RCV Id: RCV003883455

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Ser3Thr
CA367398738
NM_001354802.1:c.7T>A