Canonical Allele Identifier: PA1139699419
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 854163
ClinVar RCV Id: RCV001059146

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Val2854Phe
CA366955127
NM_001277115.2:c.8560G>T