Canonical Allele Identifier: PA645378078
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 359690
ClinVar RCV Id: RCV000383936 RCV001557906
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Pro4201Ser
CA4183130
NM_001277115.2:c.12601C>T