Canonical Allele Identifier: PA645377281
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 410828
ClinVar RCV Id: RCV000468667 RCV002293442 RCV003144272
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Met1578Ile
CA4180152
NM_001277115.2:c.4734G>C
CA366934102
NM_001277115.2:c.4734G>T
CA366934103
NM_001277115.2:c.4734G>A