Canonical Allele Identifier: PA2830287429
Gene: LRTOMT HGNC NCBI

Linked Data

ClinVar Variation Id: 305988
ClinVar RCV Id: RCV000349538
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660352.1:p.Arg116His
CA6168223
NM_145309.6:c.347G>A