Canonical Allele Identifier: PA658664902
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 454716

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Ala2957Gly
CA4181765
NM_001277115.2:c.8870C>G