Canonical Allele Identifier: PA175719
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 163104
ClinVar RCV Id: RCV000150435 RCV000556593 RCV001263479
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Arg1627Cys
CA175718
NM_001277115.2:c.4879C>T