Canonical Allele Identifier: PA658664982
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 454646
ClinVar RCV Id: RCV000543523 RCV004541639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Ala3975Val
CA4182919
NM_001277115.2:c.11924C>T