Canonical Allele Identifier: PA645377947
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 410863

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Ile3744Met
CA4182675
NM_001277115.2:c.11232C>G