Allele Registry

Canonical Allele Identifier: PA1139684798

Gene: LOXHD1 HGNC NCBI

ClinVar Variation Id: 891649

HGVS (amino-acid)	Matching Registered Transcripts
NP_001138944.1:p.Glu442Lys	CA8952316 NM_001145472.3:c.1324G>A