Canonical Allele Identifier: PA316847
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 206602
ClinVar RCV Id: RCV000188667 RCV001348402 RCV001814096 RCV003226244 RCV001847837
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002684.1:p.Met603Thr
CA316846
NM_002693.3:c.1808T>C