Canonical Allele Identifier: PA645376852
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 359600
ClinVar RCV Id: RCV000345115

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Met282Thr
CA4178794
NM_001277115.2:c.845T>C