Canonical Allele Identifier: PA658664835
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 454674
ClinVar RCV Id: RCV000532813
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Arg1408Ser
CA4179939
NM_001277115.2:c.4224G>T
CA366952401
NM_001277115.2:c.4224G>C