Canonical Allele Identifier: PA2826569851
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2723335
ClinVar RCV Id: RCV003538004
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Phe929Leu
CA4179436
NM_001277115.2:c.2787C>G
CA366944406
NM_001277115.2:c.2785T>C
CA366944411
NM_001277115.2:c.2787C>A