Canonical Allele Identifier: PA645378140
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 359699

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Val4467Met
CA4183481
NM_001277115.2:c.13399G>A