Canonical Allele Identifier: PA2826569396
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1745668
ClinVar RCV Id: RCV002338260
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Ser172Ala
CA366932249
NM_001277115.2:c.514T>G