Canonical Allele Identifier: PA916050226
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804850
ClinVar RCV Id: RCV000992056

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Arg192Gly
CA367401531
NM_033507.3:c.574C>G