Canonical Allele Identifier: PA2826569844
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2914134
ClinVar RCV Id: RCV003652904
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Ile923Val
CA4179425
NM_001277115.2:c.2767A>G