Canonical Allele Identifier: PA325088
Gene: DLAT HGNC NCBI

Linked Data

ClinVar Variation Id: 214293
ClinVar RCV Id: RCV000200505 RCV001531762 RCV002517207
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001922.2:p.Pro195Ser
CA325087
NM_001931.5:c.583C>T