Canonical Allele Identifier: PA645377140
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 359620
ClinVar RCV Id: RCV000378405

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Asp1141Val
CA4179613
NM_001277115.2:c.3422A>T