Allele Registry

Canonical Allele Identifier: PA645377123

Gene: DNAH11 HGNC NCBI

ClinVar Variation Id: 238908

HGVS (amino-acid)	Matching Registered Transcripts
NP_001264044.1:p.Met1096Ile	CA4179588 NM_001277115.2:c.3288G>A CA366945878 NM_001277115.2:c.3288G>C CA366945881 NM_001277115.2:c.3288G>T