Canonical Allele Identifier: PA176673
Gene: LRTOMT HGNC NCBI

Linked Data

ClinVar Variation Id: 163941
ClinVar RCV Id: RCV000150998

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138780.1:p.His55Gln
CA176672
NM_001145308.4:c.165C>G
CA381717244
NM_001145308.4:c.165C>A