Canonical Allele Identifier: PA2825888395
Gene: LRTOMT HGNC NCBI

Linked Data

ClinVar Variation Id: 226718

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138779.1:p.Gly118Arg
CA6168226
NM_001145307.4:c.352G>C
CA381721397
NM_001145307.4:c.352G>A