Canonical Allele Identifier: PA2827936975
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2581305
ClinVar RCV Id: RCV003331710

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Arg392Ser
CA367398628
NM_001354800.1:c.1174C>A