Canonical Allele Identifier: PA645377814
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 359661
ClinVar RCV Id: RCV000289296 RCV002272215 RCV003437126
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Ser2963Tyr
CA4181771
NM_001277115.2:c.8888C>A