Canonical Allele Identifier: CA340921

Gene:

Linked Data

• ClinVar Variation Id: 9565
• ClinVar RCV Id: RCV000010179 ; RCV003162229
• dbSNP Id: rs199474820
• MyVariant Identifiers: chrMT:g.7510T>C (hg38)
• PubMed: PMID:10978361 ; PMID:20301595
• ERepo: CA340921/MONDO:0044970/014

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.7510T>C , J01415.2:m.7510T>C	GRCh38