Canonical Allele Identifier: PA2829790940
Gene: DHX30 HGNC NCBI

Linked Data

ClinVar Variation Id: 2579793
ClinVar RCV Id: RCV003328768

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055781.2:p.Val769Glu
CA352590671
NM_014966.3:c.2306T>A