Canonical Allele Identifier: PA915982842
Gene: LRTOMT HGNC NCBI

Linked Data

ClinVar Variation Id: 44039

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138782.1:p.Val78Ile
CA133444
NM_001145310.4:c.232G>A