Canonical Allele Identifier: PA915982829
Gene: LRTOMT HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138782.1:p.Glu70Lys
CA251498
NM_001145310.4:c.208G>A