Canonical Allele Identifier: PA2826569426
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2560286
ClinVar RCV Id: RCV004327880
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Arg208Gly
CA366932531
NM_001277115.2:c.622A>G