Canonical Allele Identifier: PA2826278489
Gene: LRTOMT HGNC NCBI

Linked Data

ClinVar Variation Id: 3039178
ClinVar RCV Id: RCV003914509
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001192067.1:p.Asn119Asp
CA381721705
NM_001205138.4:c.355A>G