Canonical Allele Identifier: PA658818204
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 501278
ClinVar RCV Id: RCV000596799 RCV002532576
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Asn3347Lys
CA4182214
NM_001277115.2:c.10041T>A
CA366943647
NM_001277115.2:c.10041T>G