Canonical Allele Identifier: PA204013
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 65665
ClinVar RCV Id: RCV000055881 RCV000118011 RCV000186556 RCV000223970 RCV000229511 RCV000768289 RCV001352901 RCV001117969 RCV001847644 RCV002311532 RCV003985725
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002684.1:p.Gly517Val
CA204012
NM_002693.3:c.1550G>T