Canonical Allele Identifier: PA645377327
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 410835
ClinVar RCV Id: RCV000458384
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Phe1628Leu
CA4180209
NM_001277115.2:c.4884C>G
CA155069873
NM_001277115.2:c.4882T>C
CA366934526
NM_001277115.2:c.4884C>A