Canonical Allele Identifier: PA2826569829
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2712728
ClinVar RCV Id: RCV003537593
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Phe895Leu
CA366943758
NM_001277115.2:c.2683T>C
CA366943770
NM_001277115.2:c.2685C>A
CA366943772
NM_001277115.2:c.2685C>G