Canonical Allele Identifier: PA645377499
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 410873
ClinVar RCV Id: RCV000471454
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Ala2176Val
CA4180855
NM_001277115.2:c.6527C>T