Canonical Allele Identifier: PA645377740
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 359657

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Ser2841Gly
CA4181635
NM_001277115.2:c.8521A>G