Canonical Allele Identifier: PA179978
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 167001
ClinVar RCV Id: RCV000153158 RCV000344393
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Pro3801Arg
CA179977
NM_001277115.2:c.11402C>G