Canonical Allele Identifier: PA658818171
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 525220
ClinVar RCV Id: RCV000629268 RCV001555784
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Leu2698Ser
CA4181457
NM_001277115.2:c.8093T>C