Canonical Allele Identifier: PA2825311791
Gene: LAT HGNC NCBI
ClinVar RCV:
RCV003013120
ClinVar Variation:
2090473
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001014987.1:p.Ser40Phe
CA7989833
NM_001014987.2:c.119C>T