Canonical Allele Identifier: PA179974
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 166998
ClinVar RCV Id: RCV000153155 RCV000196489 RCV002466448 RCV001535047
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264044.1:p.Ile214Val
CA179973
NM_001277115.2:c.640A>G