Canonical Allele Identifier: PA645378123
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 359696
ClinVar RCV Id: RCV000270231

Amino-acid Alleles

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