Canonical Allele Identifier: PA316868
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 206614
ClinVar RCV Id: RCV000188680
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002684.1:p.Leu1109Val
CA316867
NM_002693.3:c.3325T>G