Canonical Allele Identifier: CA254837
Gene:

Linked Data

ClinVar Variation Id: 9583
ClinVar RCV Id: RCV000010200 RCV003162233
dbSNP Id: rs118192101
MyVariant Identifiers: chrMT:g.8313G>A (hg38)
PubMed: PMID:9380435
ERepo: CA254837/MONDO:0044970/014
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8313G>A , J01415.2:m.8313G>A GRCh38
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