Canonical Allele Identifier: PA256886
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 13498
ClinVar RCV Id: RCV000014445

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002684.1:p.Arg3Pro
CA256885
NM_002693.3:c.8G>C