Canonical Allele Identifier: PA645376800
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 238911
ClinVar RCV Id: RCV000232706 RCV002503903
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Ala113Glu
CA4178653
NM_001277115.2:c.338C>A