Canonical Allele Identifier: PA2827936898
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1933344
ClinVar RCV Id: RCV002635959

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ser360Trp
CA367399110
NM_001354800.1:c.1079C>G