Canonical Allele Identifier: PA101887
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 279982
ClinVar RCV Id: RCV000261805 RCV000678828 RCV000547242 RCV000626194 RCV001263147
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119603.1:p.Arg807Cys
CA7724495
NM_001126131.2:c.2419C>T