Canonical Allele Identifier: PA2826571416
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1774094
ClinVar RCV Id: RCV002390011
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Gly3472Arg
CA366948380
NM_001277115.2:c.10414G>A
CA366948382
NM_001277115.2:c.10414G>C