Canonical Allele Identifier: PA645376920
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 410830

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Ala567Gly
CA4179063
NM_001277115.2:c.1700C>G