Canonical Allele Identifier: PA645377843
Gene: DNAH11 HGNC NCBI
ClinVar RCV:
RCV000458967
ClinVar Variation:
410880
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Tyr3059Ser
CA4181894
NM_001277115.2:c.9176A>C