Canonical Allele Identifier: PA338133
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 215427
ClinVar RCV Id: RCV000198716 RCV000252558 RCV003437003
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Met221Leu
CA338132
NM_001277115.2:c.661A>T
CA366932606
NM_001277115.2:c.661A>C