Canonical Allele Identifier: PA174389
Gene: DNAH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 161580
ClinVar RCV Id: RCV000149115
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363.2:p.Ile1062Val
CA174388
NM_001372.4:c.3184A>G