Canonical Allele Identifier: CA120536
Gene:

Linked Data

ClinVar Variation Id: 9548
ClinVar RCV Id: RCV000010156 RCV000850660 RCV002260583
dbSNP Id: rs199476143
MyVariant Identifiers: chrMT:g.1606G>A (hg38)
ERepo: CA120536/MONDO:0044970/014
PubMed: PMID:9450773 PMID:12056939
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.1606G>A , J01415.2:m.1606G>A GRCh38
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