Canonical Allele Identifier: PA913193582
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 619328
ClinVar RCV Id: RCV000758309

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002684.1:p.Ser863Arg
CA10602234
NM_002693.3:c.2589C>G
CA393754184
NM_002693.3:c.2589C>A
CA393754197
NM_002693.3:c.2587A>C