Canonical Allele Identifier: PA355718
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 219980
ClinVar RCV Id: RCV000205270
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Ile3303Val
CA349446
NM_001277115.2:c.9907A>G