Canonical Allele Identifier: PA645377904
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 359671
ClinVar RCV Id: RCV000281061
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Lys3374Arg
CA4182236
NM_001277115.2:c.10121A>G