Canonical Allele Identifier: PA645377422
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 359640
ClinVar RCV Id: RCV000337723 RCV000606454
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Thr2051Met
CA4180699
NM_001277115.2:c.6152C>T