Canonical Allele Identifier: PA2573259048
Gene: LAT HGNC NCBI
ClinVar RCV:
RCV001902281
ClinVar Variation:
1363478
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055202.1:p.Arg93Gln
CA7989921
NM_014387.4:c.278G>A