Canonical Allele Identifier: PA2829399833
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 3068992
ClinVar RCV Id: RCV003995052
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002684.1:p.Thr929Ser
CA393753123
NM_002693.3:c.2786C>G
CA393753127
NM_002693.3:c.2785A>T