Canonical Allele Identifier: PA645377765
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 410833
ClinVar RCV Id: RCV000463577
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Gly2855Arg
CA16612081
NM_001277115.2:c.8563G>A
CA366955133
NM_001277115.2:c.8563G>C