Canonical Allele Identifier: PA316878
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 206619
ClinVar RCV Id: RCV000461638 RCV000727081 RCV000768048 RCV001804925 RCV002317148
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002684.1:p.His110Tyr
CA316877
NM_002693.3:c.328C>T