Allele Registry

Canonical Allele Identifier: PA2825786289

Gene: PDHX HGNC NCBI

ClinVar RCV:

RCV000197652

ClinVar Variation:

214967

HGVS (amino-acid)	Matching Registered Transcripts
NP_001128496.2:p.Asn359Ser	CA322110 NM_001135024.2:c.1076A>G