Canonical Allele Identifier: PA658818035
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 525289
ClinVar RCV Id: RCV000629342
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Gly269Val
CA4178783
NM_001277115.2:c.806G>T