Canonical Allele Identifier: PA2826569883
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2731861
ClinVar RCV Id: RCV003539269

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Gln986Arg
CA4179475
NM_001277115.2:c.2957A>G