Canonical Allele Identifier: PA658664849
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 454687

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Ala1890Gly
CA4180511
NM_001277115.2:c.5669C>G