Canonical Allele Identifier: PA2828965420
Gene: LOXHD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 891649

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001371403.1:p.Glu1553Lys
CA8952316
NM_001384474.1:c.4657G>A