Canonical Allele Identifier: PA176675
Gene: LRTOMT HGNC NCBI

Linked Data

ClinVar Variation Id: 163944
ClinVar RCV Id: RCV000150999 RCV002051818
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138780.1:p.Ile282Leu
CA176674
NM_001145308.4:c.844A>C
CA381727444
NM_001145308.4:c.844A>T