Canonical Allele Identifier: PA2825312020
Gene: LAT HGNC NCBI

Linked Data

ClinVar Variation Id: 1363478
ClinVar RCV Id: RCV001902281
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001014988.1:p.Arg92Gln
CA7989921
NM_001014988.2:c.275G>A