Canonical Allele Identifier: PA645376843
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 359598
ClinVar RCV Id: RCV000320459 RCV001573593
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Pro232Leu
CA4178761
NM_001277115.2:c.695C>T