Canonical Allele Identifier: PA645378062
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 281622
ClinVar RCV Id: RCV000279310 RCV001078867 RCV001161099
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Thr4170Ser
CA4183111
NM_001277115.2:c.12509C>G
CA366952747
NM_001277115.2:c.12508A>T