Canonical Allele Identifier: PA2741997619
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2684212
ClinVar RCV Id: RCV003482708

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Asp248Glu
CA367400652
NM_033507.3:c.744C>A
CA367400653
NM_033507.3:c.744C>G