Allele Registry

Canonical Allele Identifier: PA2828463881

Gene: DLAT HGNC NCBI

ClinVar RCV:

RCV000116877

RCV000676203

RCV001510014

ClinVar Variation:

128897

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358967.1:p.Ala43Val	CA152574 NM_001372038.1:c.128C>T