Canonical Allele Identifier: PA104988
Gene: LRTOMT HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138780.1:p.Glu110Lys
CA251498
NM_001145308.4:c.328G>A