Canonical Allele Identifier: PA645378017
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 227317
ClinVar RCV Id: RCV000215582 RCV000536515 RCV001162552
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Ala4059Thr
CA4182980
NM_001277115.2:c.12175G>A