Canonical Allele Identifier: PA2826571401
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2072866
ClinVar RCV Id: RCV002967429
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Met3458Val
CA4182346
NM_001277115.2:c.10372A>G