Canonical Allele Identifier: PA658664878
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 454704
ClinVar RCV Id: RCV000553275
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Arg2432Gln
CA4181183
NM_001277115.2:c.7295G>A