Canonical Allele Identifier: PA2827937087
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1933344
ClinVar RCV Id: RCV002635959
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Ser23Trp
CA367399110
NM_001354801.1:c.68C>G