Canonical Allele Identifier: CA658799929

Gene:

Linked Data

• ClinVar Variation Id: 505138
• ClinVar RCV Id: RCV000615679
• dbSNP Id: rs1556422500
• MyVariant Identifiers: chrMT:g.962C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.962C>T , J01415.2:m.962C>T	GRCh38