Canonical Allele Identifier: PA645376775
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 410866
ClinVar RCV Id: RCV000476838
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Arg60Pro
CA4178626
NM_001277115.2:c.179G>C