Canonical Allele Identifier: PA2826569397
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 3013704
ClinVar RCV Id: RCV003873279
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Lys174Asn
CA366932288
NM_001277115.2:c.522G>C
CA366932289
NM_001277115.2:c.522G>T