Canonical Allele Identifier: PA2830285334
Gene: LOXHD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 891649

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653213.6:p.Glu1553Lys
CA8952316
NM_144612.7:c.4657G>A