Canonical Allele Identifier: PA658664930
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 454723
ClinVar RCV Id: RCV000543160
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Gly3295Asp
CA4182141
NM_001277115.2:c.9884G>A