Canonical Allele Identifier: PA355058
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 221194
ClinVar RCV Id: RCV000203756 RCV000214432 RCV000514577
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Asp4187Glu
CA348046
NM_001277115.2:c.12561T>G
CA366952985
NM_001277115.2:c.12561T>A