Canonical Allele Identifier: PA256892
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 13500
ClinVar RCV Id: RCV000014454 RCV000758263 RCV001797046
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002684.1:p.His932Tyr
CA256891
NM_002693.3:c.2794C>T