Canonical Allele Identifier: PA645377332
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 359629
ClinVar RCV Id: RCV000287520
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Val1631Ile
CA4180212
NM_001277115.2:c.4891G>A