Canonical Allele Identifier: PA658664986
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 454649

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Pro4110Thr
CA4183036
NM_001277115.2:c.12328C>A