Canonical Allele Identifier: PA2826571044
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 3017043
ClinVar RCV Id: RCV003871162
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Leu2894Ile
CA366955671
NM_001277115.2:c.8680C>A