Canonical Allele Identifier: PA915982827
Gene: LRTOMT HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138782.1:p.Trp65Arg
CA251497
NM_001145310.4:c.193T>C
CA381718166
NM_001145310.4:c.193T>A