Canonical Allele Identifier: PA645376823
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 359596
ClinVar RCV Id: RCV000354120 RCV003437124
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Tyr190Phe
CA4178715
NM_001277115.2:c.569A>T