Canonical Allele Identifier: PA2825312192
Gene: LAT HGNC NCBI

Linked Data

ClinVar Variation Id: 1363478
ClinVar RCV Id: RCV001902281
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001014989.2:p.Arg129Gln
CA7989921
NM_001014989.2:c.386G>A