Canonical Allele Identifier: PA316807
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 206581
ClinVar RCV Id: RCV000633538 RCV000678826 RCV000710188 RCV001121513 RCV001263148 RCV001808471 RCV002362986 RCV003317141
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002684.1:p.Gln226His
CA316806
NM_002693.3:c.678G>C
CA393767261
NM_002693.3:c.678G>T