Canonical Allele Identifier: PA2828462101
Gene: DLAT HGNC NCBI

Linked Data

ClinVar Variation Id: 418162
ClinVar RCV Id: RCV000481071
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358962.1:p.Phe137Cys
CA6276663
NM_001372033.1:c.410T>G