Canonical Allele Identifier: PA645377979
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 359679

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Gly3849Val
CA4182793
NM_001277115.2:c.11546G>T