Allele Registry

Canonical Allele Identifier: PA358664

Gene: DDX41 HGNC NCBI

ClinVar RCV:

RCV000210262

RCV001553497

ClinVar Variation:

224635

HGVS (amino-acid)	Matching Registered Transcripts
NP_057306.2:p.Ile396Thr	CA358663 NM_016222.3:c.1187T>C