Canonical Allele Identifier: PA102078
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 13502
ClinVar RCV Id: RCV000014449 RCV000014450 RCV000014451 RCV000014452 RCV000188580 RCV000363602 RCV000515163 RCV000678386 RCV001027839 RCV002054437 RCV002272018 RCV002313707 RCV001847601 RCV003231103 RCV003230362
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119603.1:p.Gly848Ser
CA123144
NM_001126131.2:c.2542G>A