Canonical Allele Identifier: PA316835
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 206596
ClinVar RCV Id: RCV000470781 RCV000678827 RCV001027840 RCV000763995 RCV001117972 RCV000658725 RCV001004603 RCV001330959 RCV001610504 RCV001263305 RCV001847836 RCV002314743 RCV003230444
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002684.1:p.Asn468Asp
CA316834
NM_002693.3:c.1402A>G