Canonical Allele Identifier: PA658664988
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 454650
ClinVar RCV Id: RCV000536426
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Ile4115Ser
CA4183040
NM_001277115.2:c.12344T>G