Canonical Allele Identifier: PA645376829
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 284312
ClinVar RCV Id: RCV000279404 RCV001314631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.His191Tyr
CA4178716
NM_001277115.2:c.571C>T