Canonical Allele Identifier: PA645377015
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 359615
ClinVar RCV Id: RCV000272070
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Lys835Arg
CA4179359
NM_001277115.2:c.2504A>G