Canonical Allele Identifier: PA645377613
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 359652
ClinVar RCV Id: RCV000284216 RCV002504178 RCV002264932
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Val2518Ala
CA4181262
NM_001277115.2:c.7553T>C