Canonical Allele Identifier: PA645377582
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 257927
ClinVar RCV Id: RCV000245120 RCV001854957
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Ser2445Leu
CA4181195
NM_001277115.2:c.7334C>T