ClinGen Allele Registry
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Canonical Allele Identifier:
CA645373344
Gene:
Linked Data
ClinVar Variation Id:
430688
ClinVar RCV Id:
RCV000495226
dbSNP Id:
rs1131692062
MyVariant Identifiers:
chrMT:g.12283G>A (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.12283G>A , J01415.2:m.12283G>A
GRCh38
Search 100 bp 5'
Search 100 bp 3'