Canonical Allele Identifier: PA2580490847
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1700684
ClinVar RCV Id: RCV002285562

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Ile294Arg
CA367400163
NM_033507.3:c.881T>G