Allele Registry

Canonical Allele Identifier: PA316813

Gene: POLG HGNC NCBI

ClinVar RCV:

RCV000188644

RCV000758410

ClinVar Variation:

206584

HGVS (amino-acid)	Matching Registered Transcripts
NP_002684.1:p.Gln285His	CA316812 NM_002693.3:c.855G>C CA393766494 NM_002693.3:c.855G>T