Canonical Allele Identifier: CA120566
Gene:

Linked Data

ClinVar Variation Id: 9596
ClinVar RCV Id: RCV000010219 RCV000850698
dbSNP Id: rs199474663
MyVariant Identifiers: chrMT:g.3260A>G (hg38)
PubMed: PMID:1677065 PMID:8132749
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3260A>G , J01415.2:m.3260A>G GRCh38
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