Canonical Allele Identifier: PA2826569836
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 3016551
ClinVar RCV Id: RCV003878686

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Lys905Thr
CA4179413
NM_001277115.2:c.2714A>C