Canonical Allele Identifier: PA175744
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 163118

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Asp3312Val
CA175743
NM_001277115.2:c.9935A>T