Canonical Allele Identifier: PA2573192214
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1446166
ClinVar RCV Id: RCV001992765
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Gly3523Val
CA366949309
NM_001277115.2:c.10568G>T