Allele Registry

Canonical Allele Identifier: PA316849

Gene: POLG HGNC NCBI

ClinVar Allele:

202999

ClinVar RCV:

RCV000188668

RCV001336494

ClinVar Variation:

206603

HGVS (amino-acid)	Matching Registered Transcripts
NP_002684.1:p.Leu623Trp	CA316848 NM_002693.3:c.1868T>G