Canonical Allele Identifier: PA645377942
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 410870
ClinVar RCV Id: RCV000470004
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Leu3722Pro
CA16612187
NM_001277115.2:c.11165T>C