Allele Registry

Canonical Allele Identifier: PA316767

Gene: POLG HGNC NCBI

ClinVar RCV:

RCV000188618

RCV000552872

RCV003230443

ClinVar Variation:

206561

HGVS (amino-acid)	Matching Registered Transcripts
NP_002684.1:p.Met1116Val	CA316766 NM_002693.3:c.3346A>G