Canonical Allele Identifier: PA645377762
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 359658

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Arg2845Gly
CA4181638
NM_001277115.2:c.8533C>G