Allele Registry

Canonical Allele Identifier: PA2828464612

Gene: DLAT HGNC NCBI

ClinVar RCV:

RCV000116879

RCV000676208

RCV001516164

ClinVar Variation:

128899

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358969.1:p.Val191Ala	CA152578 NM_001372040.1:c.572T>C CA3054209091 NM_001372040.1:c.572_573delinsCA