Canonical Allele Identifier: PA316787
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 206571
ClinVar RCV Id: RCV000188628 RCV001847833 RCV000758333
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002684.1:p.Asp1196Asn
CA316786
NM_002693.3:c.3586G>A