Canonical Allele Identifier: PA645377451
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 238928

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Asn2101Ser
CA4180777
NM_001277115.2:c.6302A>G