Canonical Allele Identifier: PA645377214
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 238915
ClinVar RCV Id: RCV000227209

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Arg1375His
CA4179909
NM_001277115.2:c.4124G>A