Canonical Allele Identifier: PA645377498
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 410879
ClinVar RCV Id: RCV000477052 RCV002470864
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Val2172Leu
CA16612170
NM_001277115.2:c.6514G>C
CA366938185
NM_001277115.2:c.6514G>T