Canonical Allele Identifier: PA645377212
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 432277
ClinVar RCV Id: RCV000498937 RCV003535787
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Ile1334Val
CA4179836
NM_001277115.2:c.4000A>G