Canonical Allele Identifier: PA105013
Gene: LRTOMT HGNC NCBI
ClinVar RCV:
RCV000000574
ClinVar Variation:
544
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138780.1:p.Trp105Arg
CA251497
NM_001145308.4:c.313T>C
CA381718166
NM_001145308.4:c.313T>A