Canonical Allele Identifier: PA916030222
Gene: DDX59 HGNC NCBI

Linked Data

ClinVar Variation Id: 88653
ClinVar RCV Id: RCV000433647 RCV000074347
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336731.1:p.Val367Gly
CA145273
NM_001349802.3:c.1100T>G