Canonical Allele Identifier: PA645377935
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 359675

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Asn3694Ile
CA4182613
NM_001277115.2:c.11081A>T