Canonical Allele Identifier: PA185732
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 180063
ClinVar RCV Id: RCV000156866 RCV001392556
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Arg2146His
CA185731
NM_001277115.2:c.6437G>A