Canonical Allele Identifier: CA337095942
Gene:

Linked Data

dbSNP Id: rs2853519
MyVariant Identifiers: chrMT:g.769G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.769G>A , J01415.2:m.769G>A GRCh38
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