Allele Registry

Canonical Allele Identifier: PA322111

Gene: PDHX HGNC NCBI

ClinVar RCV:

RCV000197652

ClinVar Variation:

214967

HGVS (amino-acid)	Matching Registered Transcripts
NP_003468.2:p.Asn419Ser	CA322110 NM_003477.3:c.1256A>G