Canonical Allele Identifier: PA316818
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 206587

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002684.1:p.Arg288His
CA316817
NM_002693.3:c.863G>A