Canonical Allele Identifier: PA316820
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 206588
ClinVar RCV Id: RCV000188649 RCV000758271 RCV000995844 RCV001332170 RCV002372152
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002684.1:p.Ser305Arg
CA316819
NM_002693.3:c.915C>G
CA393765813
NM_002693.3:c.915C>A
CA393765820
NM_002693.3:c.913A>C