Canonical Allele Identifier: PA292864
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 21320
ClinVar RCV Id: RCV000127555 RCV000468571 RCV000710190 RCV001121509 RCV001847613 RCV002371780
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002684.1:p.Pro324Ser
CA292863
NM_002693.3:c.970C>T