Canonical Allele Identifier: PA2827936819
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2632747
ClinVar RCV Id: RCV003408314

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Gln287Glu
CA367400409
NM_001354800.1:c.859C>G