Canonical Allele Identifier: PA175742
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 163117
ClinVar RCV Id: RCV000150448 RCV000205997 RCV001705981 RCV003114294
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Ile3033Val
CA175741
NM_001277115.2:c.9097A>G