Canonical Allele Identifier: PA295635
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 167522
ClinVar RCV Id: RCV000153756 RCV000676330 RCV000714693 RCV000758545 RCV001847785 RCV002492575 RCV002312681 RCV003993835
ClinVar Variation Id: 206483
ClinVar RCV Id: RCV000188533 RCV000876734 RCV001492580
ClinVar Variation Id: 1056216
ClinVar RCV Id: RCV001365007
ClinVar Variation Id: 1470676
ClinVar RCV Id: RCV001964294
ClinVar Variation Id: 2416706
ClinVar RCV Id: RCV003108957
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002684.1:p.Gln55dup
CA316620
NM_002693.3:c.159_161dup
CA2194573149
NM_002693.3:c.164_166dup
CA2998560047
NM_002693.3:c.164_165insACA