Canonical Allele Identifier: CA120583
Gene:

Linked Data

ClinVar Variation Id: 9620
ClinVar RCV Id: RCV000010245 RCV002247296 RCV003162236
dbSNP Id: rs199476130
MyVariant Identifiers: chrMT:g.5703G>A (hg38)
ERepo: CA120583/MONDO:0044970/014
PubMed: PMID:8254046 PMID:9372914 PMID:14518831
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5703G>A , J01415.2:m.5703G>A GRCh38
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