Canonical Allele Identifier: PA2825888579
Gene: LRTOMT HGNC NCBI

Linked Data

ClinVar Variation Id: 228842

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138782.1:p.His228Tyr
CA6168646
NM_001145310.4:c.682C>T