Allele Registry

Canonical Allele Identifier: PA2826026069

Gene: PDHX HGNC NCBI

ClinVar RCV:

RCV000197652

ClinVar Variation:

214967

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159630.1:p.Asn192Ser	CA322110 NM_001166158.2:c.575A>G