Canonical Allele Identifier: PA645376878
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 410843
ClinVar RCV Id: RCV000468824 RCV001160009 RCV002274035
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Tyr378Ser
CA4178908
NM_001277115.2:c.1133A>C