Canonical Allele Identifier: CA254844
Gene:

Linked Data

ClinVar Variation Id: 9616
ClinVar RCV Id: RCV000010240 RCV003162235
dbSNP Id: rs199476141
MyVariant Identifiers: chrMT:g.4332G>A (hg38)
ERepo: CA254844/MONDO:0044970/014
PubMed: PMID:11171912
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4332G>A , J01415.2:m.4332G>A GRCh38
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