Canonical Allele Identifier: PA316811
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 206583
ClinVar RCV Id: RCV000188643 RCV000396333 RCV000231645 RCV000616176 RCV001004406 RCV001847834 RCV002514036 RCV002226693 RCV003235111
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002684.1:p.His277Leu
CA316810
NM_002693.3:c.830A>T