Canonical Allele Identifier: PA645404189
Gene: DHX30 HGNC NCBI

Linked Data

ClinVar Variation Id: 426111
ClinVar RCV Id: RCV000489269 RCV000546135 RCV001266616
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_619520.1:p.Arg785Cys
CA352590365
NM_138615.2:c.2353C>T