Canonical Allele Identifier: PA645378123
Gene: DNAH11 HGNC NCBI
ClinVar RCV:
RCV000270231
ClinVar Variation:
359696
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Pro4421Leu
CA4183385
NM_001277115.2:c.13262C>T