Canonical Allele Identifier: PA2825311970
Gene: LAT HGNC NCBI

Linked Data

ClinVar Variation Id: 2090473
ClinVar RCV Id: RCV003013120
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001014988.1:p.Ser40Phe
CA7989833
NM_001014988.2:c.119C>T