Canonical Allele Identifier: PA645377737
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 376823

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Leu2779Met
CA4181574
NM_001277115.2:c.8335C>A