Canonical Allele Identifier: PA645377150
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 359622
ClinVar RCV Id: RCV000393983
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.His1166Pro
CA4179658
NM_001277115.2:c.3497A>C