Canonical Allele Identifier: PA2499235185
Gene: LAT HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001014989.2:p.Asp73Asn
CA7989830
NM_001014989.2:c.217G>A