Canonical Allele Identifier: PA2826569889
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1798324
ClinVar RCV Id: RCV002442138
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Thr992Ile
CA4179481
NM_001277115.2:c.2975C>T