Canonical Allele Identifier: PA2826570179
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2727278
ClinVar RCV Id: RCV003539035

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Ala1451Val
CA4180001
NM_001277115.2:c.4352C>T