Canonical Allele Identifier: PA2579981585
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2632747
ClinVar RCV Id: RCV003408314

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Gln287Glu
CA367400409
NM_000162.5:c.859C>G