Canonical Allele Identifier: CA337095804
Gene:
ClinVar RCV:
RCV000509228
ClinVar Variation:
441147
dbSNP:
2853515
MyVariant.info:
GRCh38 chrMT:g.263A>G
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.263A>G , J01415.2:m.263A>G GRCh38
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