Canonical Allele Identifier: PA256886
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 13498
ClinVar RCV Id: RCV000014445
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002684.1:p.Arg3Pro
CA256885
NM_002693.3:c.8G>C