Canonical Allele Identifier: PA2827074695
Gene: DDX41 HGNC NCBI

Linked Data

ClinVar Variation Id: 1313715
ClinVar RCV Id: RCV001769361
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308661.1:p.Pro308Leu
CA3584820
NM_001321732.2:c.923C>T