Canonical Allele Identifier: PA645377174
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 416418
ClinVar RCV Id: RCV000475932 RCV003105916
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Glu1290Asp
CA4179811
NM_001277115.2:c.3870G>C
CA366951046
NM_001277115.2:c.3870G>T