Allele Registry

Canonical Allele Identifier: PA2828964047

Gene: LOXHD1 HGNC NCBI

ClinVar Variation Id: 891861

HGVS (amino-acid)	Matching Registered Transcripts
NP_001371403.1:p.Phe599Leu	CA8952760 NM_001384474.1:c.1795T>C CA402378882 NM_001384474.1:c.1797T>A CA402378883 NM_001384474.1:c.1797T>G