Canonical Allele Identifier: PA2826569861
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2727221
ClinVar RCV Id: RCV003539032
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Pro940Leu
CA4179443
NM_001277115.2:c.2819C>T