Canonical Allele Identifier: PA2825311789
Gene: LAT HGNC NCBI

Linked Data

ClinVar Variation Id: 1038087
ClinVar RCV Id: RCV001341348
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001014987.1:p.Asp37Asn
CA7989830
NM_001014987.2:c.109G>A