Canonical Allele Identifier: PA2827936559
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1346275
ClinVar RCV Id: RCV002029930
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ser151Tyr
CA367401935
NM_001354800.1:c.452C>A