Canonical Allele Identifier: PA182892
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 178725
ClinVar RCV Id: RCV000155485 RCV000274400 RCV001538163 RCV001657883
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Val1023Ala
CA182891
NM_001277115.2:c.3068T>C