Canonical Allele Identifier: PA248707
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 21312
ClinVar RCV Id: RCV000020476 RCV000118018 RCV000386578 RCV000469563 RCV000676317 RCV000755650 RCV000999632 RCV001119316 RCV002311518 RCV001847611
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002684.1:p.Glu1143Gly
CA248706
NM_002693.3:c.3428A>G