Canonical Allele Identifier: PA645377815
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 238937

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Arg2990His
CA4181804
NM_001277115.2:c.8969G>A