Canonical Allele Identifier: PA645378016
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 359682
ClinVar RCV Id: RCV000315398
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Lys4003Met
CA4182948
NM_001277115.2:c.12008A>T