Canonical Allele Identifier: PA916039361
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585914
ClinVar RCV Id: RCV000711765 RCV000764717 RCV003493719
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Thr57Ile
CA367397075
NM_001354802.1:c.170C>T