Allele Registry

Canonical Allele Identifier: PA316785

Gene: POLG HGNC NCBI

ClinVar RCV:

RCV000188627

RCV000633564

RCV000712805

RCV001847832

RCV002453696

RCV003985759

ClinVar Variation:

206570

HGVS (amino-acid)	Matching Registered Transcripts
NP_002684.1:p.Arg1187Trp	CA316784 NM_002693.3:c.3559C>T