Canonical Allele Identifier: PA658664868
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 450055

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Arg2189Gln
CA4180894
NM_001277115.2:c.6566G>A