Canonical Allele Identifier: PA658664828
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 454670

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Asp1165Gly
CA4179655
NM_001277115.2:c.3494A>G