Canonical Allele Identifier: PA891857513
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 576761
ClinVar RCV Id: RCV000699336

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002684.1:p.Gly1238Arg
CA274538370
NM_002693.3:c.3712G>C
CA393746798
NM_002693.3:c.3712G>A