Canonical Allele Identifier: PA645377868
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 359668

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Tyr3258Cys
CA4182112
NM_001277115.2:c.9773A>G