Canonical Allele Identifier: PA175762
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 163128
ClinVar RCV Id: RCV000150459 RCV000468438 RCV003144142 RCV004544351
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Gln4323His
CA175761
NM_001277115.2:c.12969G>C
CA4183235
NM_001277115.2:c.12969G>T