Canonical Allele Identifier: PA645376886
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 282964

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Asp407Ala
CA4178937
NM_001277115.2:c.1220A>C