Canonical Allele Identifier: PA915982809
Gene: LRTOMT HGNC NCBI

Linked Data

ClinVar Variation Id: 228842
ClinVar RCV Id: RCV000219698 RCV000341492 RCV000992285
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138781.1:p.His268Tyr
CA6168646
NM_001145309.4:c.802C>T