Canonical Allele Identifier: PA645377958
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 359677
ClinVar RCV Id: RCV000319457 RCV000764704
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Val3750Gly
CA4182679
NM_001277115.2:c.11249T>G