Canonical Allele Identifier: PA645377335
Gene: DNAH11 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Lys1655Arg
CA4180257
NM_001277115.2:c.4964A>G