Canonical Allele Identifier: PA2573175919
Gene: LAT HGNC NCBI

Linked Data

ClinVar Variation Id: 1493770
ClinVar RCV Id: RCV001986730
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001014989.2:p.Thr92Met
CA7989878
NM_001014989.2:c.275C>T