Allele Registry

Canonical Allele Identifier: PA2829790934

Gene: DHX30 HGNC NCBI

ClinVar Variation Id: 426111

HGVS (amino-acid)	Matching Registered Transcripts
NP_055781.2:p.Arg746Cys	CA352590365 NM_014966.3:c.2236C>T