Canonical Allele Identifier: PA645377337
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 226586

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Ile1718Val
CA4180322
NM_001277115.2:c.5152A>G