Canonical Allele Identifier: CA254834
Gene:

Linked Data

ClinVar Variation Id: 9573
ClinVar RCV Id: RCV000010186 RCV003153296
dbSNP Id: rs118203885
MyVariant Identifiers: chrMT:g.583G>A (hg38)
ERepo: CA254834/MONDO:0044970/014
PubMed: PMID:1171391 PMID:2102678 PMID:6093682 PMID:9771776
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.583G>A , J01415.2:m.583G>A GRCh38
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