Canonical Allele Identifier: PA113495
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 163116
ClinVar RCV Id: RCV000150447 RCV000230982 RCV001705980 RCV001729408
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Arg2997Gln
CA175740
NM_001277115.2:c.8990G>A