Canonical Allele Identifier: PA645377910
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 416427
ClinVar RCV Id: RCV001473638
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Thr3460Lys
CA4182348
NM_001277115.2:c.10379C>A