Allele Registry

Canonical Allele Identifier: PA2828462595

Gene: DLAT HGNC NCBI

ClinVar RCV:

RCV000116879

RCV000676208

RCV001516164

ClinVar Variation:

128899

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358963.1:p.Val307Ala	CA152578 NM_001372034.1:c.920T>C CA3054209091 NM_001372034.1:c.920_921delinsCA