Canonical Allele Identifier: PA302813
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 195182
ClinVar RCV Id: RCV000633544 RCV000724132 RCV000763999 RCV001252351 RCV001116627 RCV001847811 RCV004526626 RCV002453618 RCV003985740
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002684.1:p.Gly11Asp
CA302812
NM_002693.3:c.32G>A