Allele Registry

Canonical Allele Identifier: PA316635

Gene: POLG HGNC NCBI

ClinVar RCV:

RCV000469850

RCV000578205

RCV000726559

RCV001116622

RCV001252352

RCV002321761

RCV003985750

RCV003993876

ClinVar Variation:

206492

HGVS (amino-acid)	Matching Registered Transcripts
NP_002684.1:p.Tyr131His	CA316634 NM_002693.3:c.391T>C