Canonical Allele Identifier: PA645377412
Gene: DNAH11 HGNC NCBI
ClinVar RCV:
RCV000226575
ClinVar Variation:
238927
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Gly1998Asp
CA4180631
NM_001277115.2:c.5993G>A