Canonical Allele Identifier: PA246939
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 198347
ClinVar RCV Id: RCV000218296 RCV000226017 RCV000723974 RCV001160743 RCV000735289 RCV004537494
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Arg3491His
CA246938
NM_001277115.2:c.10472G>A