Canonical Allele Identifier: PA645377507
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 410855
ClinVar RCV Id: RCV000469872 RCV002056712 RCV001160315
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Pro2308Leu
CA16612073
NM_001277115.2:c.6923C>T