Canonical Allele Identifier: PA355155
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 219979
ClinVar RCV Id: RCV000203962
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Trp1410Cys
CA348241
NM_001277115.2:c.4230G>T
CA366952416
NM_001277115.2:c.4230G>C