Canonical Allele Identifier: PA2826570252
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2914426
ClinVar RCV Id: RCV003652914
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Thr1542Ala
CA4180113
NM_001277115.2:c.4624A>G