Canonical Allele Identifier: PA2573192204
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1509421
ClinVar RCV Id: RCV002040668
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Thr3460Met
CA4182349
NM_001277115.2:c.10379C>T