Canonical Allele Identifier: PA2827936743
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2684212
ClinVar RCV Id: RCV003482708

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Asp247Glu
CA367400652
NM_001354800.1:c.741C>A
CA367400653
NM_001354800.1:c.741C>G