Canonical Allele Identifier: PA2826569322
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2040497
ClinVar RCV Id: RCV002886450
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Glu40dup
CA454138892
NM_001277115.2:c.118_120dup