Canonical Allele Identifier: PA2826569847
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2067598
ClinVar RCV Id: RCV002966532
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.His925Leu
CA4179430
NM_001277115.2:c.2774A>T