Canonical Allele Identifier: PA316765
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 206560

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002684.1:p.Ala1105Pro
CA316764
NM_002693.3:c.3313G>C