Canonical Allele Identifier: PA2827937269
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804836
ClinVar RCV Id: RCV000992038 RCV002463760 RCV003396574
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Ala4Val
CA367398721
NM_001354802.1:c.11C>T