Canonical Allele Identifier: PA2829790932
Gene: DHX30 HGNC NCBI

Linked Data

ClinVar Variation Id: 2444127
ClinVar RCV Id: RCV003152925
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055781.2:p.Arg743Pro
CA352590329
NM_014966.3:c.2228G>C