Canonical Allele Identifier: PA645377008
Gene: DNAH11 HGNC NCBI
ClinVar RCV:
RCV000402697
ClinVar Variation:
359613
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Asp807His
CA4179333
NM_001277115.2:c.2419G>C