Canonical Allele Identifier: PA2825311969
Gene: LAT HGNC NCBI
ClinVar RCV:
RCV001341348
ClinVar Variation:
1038087
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001014988.1:p.Asp37Asn
CA7989830
NM_001014988.2:c.109G>A