Canonical Allele Identifier: PA2830122283
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2578359
ClinVar RCV Id: RCV003326085

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Arg398Gly
CA367398536
NM_033507.3:c.1192C>G