Canonical Allele Identifier: PA2829739211
Gene: LAT HGNC NCBI
ClinVar RCV:
RCV003013120
ClinVar Variation:
2090473
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055202.1:p.Ser40Phe
CA7989833
NM_014387.4:c.119C>T