Canonical Allele Identifier: PA2826569400
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2265991
ClinVar RCV Id: RCV003534968
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.His177Asp
CA4178705
NM_001277115.2:c.529C>G