Allele Registry

Canonical Allele Identifier: PA316775

Gene: POLG HGNC NCBI

ClinVar RCV:

RCV000188622

RCV000758478

ClinVar Variation:

206565

HGVS (amino-acid)	Matching Registered Transcripts
NP_002684.1:p.Asn1157Ser	CA316774 NM_002693.3:c.3470A>G