Canonical Allele Identifier: PA2827350844
Gene: DHX30 HGNC NCBI

Linked Data

ClinVar Variation Id: 402130
ClinVar RCV Id: RCV000454247 RCV000544652 RCV001003584
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317919.1:p.His534Arg
CA16609494
NM_001330990.2:c.1601A>G