Canonical Allele Identifier: PA645377912
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 238888

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Thr3464Ile
CA4182353
NM_001277115.2:c.10391C>T