Canonical Allele Identifier: PA658818021
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 505254
ClinVar RCV Id: RCV000606297 RCV003767441
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Ser23Leu
CA155057668
NM_001277115.2:c.68C>T