Canonical Allele Identifier: PA916007702
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 666153
ClinVar RCV Id: RCV000824587

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Arg2839His
CA366955046
NM_001277115.2:c.8516G>A