Canonical Allele Identifier: PA2825311803
Gene: LAT HGNC NCBI
ClinVar RCV:
RCV001986730
ClinVar Variation:
1493770
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001014987.1:p.Thr56Met
CA7989878
NM_001014987.2:c.167C>T