Canonical Allele Identifier: PA2825888487
Gene: LRTOMT HGNC NCBI

Linked Data

ClinVar Variation Id: 44039

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138781.1:p.Val118Ile
CA133444
NM_001145309.4:c.352G>A