Canonical Allele Identifier: PA658664886
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 454709

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Ile2675Phe
CA4181446
NM_001277115.2:c.8023A>T