Canonical Allele Identifier: PA658818111
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 525302
ClinVar RCV Id: RCV000629355
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Arg1715Cys
CA4180319
NM_001277115.2:c.5143C>T