Canonical Allele Identifier: PA2827513166
Gene: DDX59 HGNC NCBI

Linked Data

ClinVar Variation Id: 88653
ClinVar RCV Id: RCV000433647 RCV000074347
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336730.1:p.Val367Gly
CA145273
NM_001349801.3:c.1100T>G