Canonical Allele Identifier: PA916069673
Gene: DHX30 HGNC NCBI

Linked Data

ClinVar Variation Id: 523233
ClinVar RCV Id: RCV000626487 RCV001764741
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_619520.1:p.Arg908Gln
CA352591980
NM_138615.2:c.2723G>A