Canonical Allele Identifier: CA120544

Gene:

Linked Data

• ClinVar Variation Id: 9560
• ClinVar RCV Id: RCV000010170 ; RCV000010171 ; RCV003162227
• dbSNP Id: rs118203888
• MyVariant Identifiers: chrMT:g.12258C>A (hg38)
• ERepo: CA120544/MONDO:0044970/014
• PubMed: PMID:9792552 ; PMID:10090882

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12258C>A , J01415.2:m.12258C>A	GRCh38