Canonical Allele Identifier: PA645377379
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 410838
ClinVar RCV Id: RCV000457354
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Val1914Phe
CA4180530
NM_001277115.2:c.5740G>T