Canonical Allele Identifier: PA270088
Gene: LRAT HGNC NCBI

Linked Data

ClinVar Variation Id: 143129

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004735.2:p.Arg55Trp
CA270087
NM_004744.5:c.163C>T