Canonical Allele Identifier: PA645377456
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 410849

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Gly2118Ser
CA4180791
NM_001277115.2:c.6352G>A