Canonical Allele Identifier: PA645377373
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 359636
ClinVar RCV Id: RCV000272871 RCV000764702 RCV002264931
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Thr1840Ile
CA4180464
NM_001277115.2:c.5519C>T