Canonical Allele Identifier: PA645377856
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 281471

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Thr3167Pro
CA4182012
NM_001277115.2:c.9499A>C