Canonical Allele Identifier: PA355613
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 220425
ClinVar RCV Id: RCV000205041 RCV001333063 RCV001559427
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Arg2432Trp
CA349204
NM_001277115.2:c.7294C>T