Canonical Allele Identifier: CA120551
Gene:

Linked Data

ClinVar Variation Id: 9575
ClinVar RCV Id: RCV000010188 RCV002247289
dbSNP Id: rs118203887
MyVariant Identifiers: chrMT:g.622G>A (hg38)
PubMed: PMID:16769874
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.622G>A , J01415.2:m.622G>A GRCh38
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