Canonical Allele Identifier: PA2826569838
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2706386
ClinVar RCV Id: RCV003536406

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Phe910Cys
CA4179416
NM_001277115.2:c.2729T>G