Canonical Allele Identifier: PA2826571041
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2200533
ClinVar RCV Id: RCV002644155

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Tyr2885His
CA366955491
NM_001277115.2:c.8653T>C