Canonical Allele Identifier: PA2826570261
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1742334
ClinVar RCV Id: RCV002335165
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Ile1558Phe
CA366933561
NM_001277115.2:c.4672A>T