Canonical Allele Identifier: PA645377413
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 359639
ClinVar RCV Id: RCV000386425 RCV002466490
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Pro2006Leu
CA4180639
NM_001277115.2:c.6017C>T