Canonical Allele Identifier: CA130991
Gene:
ClinVar RCV:
RCV000035028
ClinVar Variation:
42204
dbSNP:
2000974
MyVariant.info:
GRCh38 chrMT:g.1048C>T
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.1048C>T , J01415.2:m.1048C>T GRCh38
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