Canonical Allele Identifier: PA645477390
Gene: LRTOMT HGNC NCBI

Linked Data

ClinVar Variation Id: 305988
ClinVar RCV Id: RCV000349538

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138779.1:p.Arg116His
CA6168223
NM_001145307.4:c.347G>A