Canonical Allele Identifier: PA916007916
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 810073
ClinVar RCV Id: RCV000998775
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.His4088Gln
CA366963995
NM_001277115.2:c.12264C>A
CA366963996
NM_001277115.2:c.12264C>G