Canonical Allele Identifier: PA2580500390
Gene: DHX30 HGNC NCBI

Linked Data

ClinVar Variation Id: 2444127
ClinVar RCV Id: RCV003152925

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_619520.1:p.Arg782Pro
CA352590329
NM_138615.2:c.2345G>C