Canonical Allele Identifier: PA645377967
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 359678

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Ile3792Val
CA4182733
NM_001277115.2:c.11374A>G