Canonical Allele Identifier: PA2826864208
Gene: LRAT HGNC NCBI

Linked Data

ClinVar Variation Id: 2259329
ClinVar RCV Id: RCV002778098
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001288574.1:p.Tyr40Ser
CA358630017
NM_001301645.2:c.119A>C