Canonical Allele Identifier: PA2826571439
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2719802
ClinVar RCV Id: RCV003537859

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Trp3505Cys
CA4182380
NM_001277115.2:c.10515G>T
CA366948967
NM_001277115.2:c.10515G>C