Canonical Allele Identifier: PA645376984
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 359609
ClinVar RCV Id: RCV000348500
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Ser684Cys
CA4179203
NM_001277115.2:c.2050A>T