Canonical Allele Identifier: CA337095938
Gene:

Linked Data

ClinVar Variation Id: 441148
ClinVar RCV Id: RCV000509422 RCV003886405
dbSNP Id: rs2853518
MyVariant Identifiers: chrMT:g.750A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.750A>G , J01415.2:m.750A>G GRCh38
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