Canonical Allele Identifier: PA645404169
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_619520.1:p.His562Arg
CA16609494
NM_138615.2:c.1685A>G