Canonical Allele Identifier: PA658664836
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 454675
ClinVar RCV Id: RCV000543304
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Arg1445Gln
CA4179998
NM_001277115.2:c.4334G>A