Canonical Allele Identifier: PA355770
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 219477
ClinVar RCV Id: RCV000205408 RCV000600436 RCV004541286 RCV000998771
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Gln1711Arg
CA349577
NM_001277115.2:c.5132A>G