Allele Registry

Canonical Allele Identifier: PA316872

Gene: POLG HGNC NCBI

ClinVar RCV:

RCV000188682

ClinVar Variation:

206616

HGVS (amino-acid)	Matching Registered Transcripts
NP_002684.1:p.Met1163Thr	CA316871 NM_002693.3:c.3488T>C