Canonical Allele Identifier: PA645377259
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 238920

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Ile1533Ser
CA4180105
NM_001277115.2:c.4598T>G