Canonical Allele Identifier: CA10581201

Gene:

Linked Data

• ClinVar Variation Id: 235013
• ClinVar RCV Id: RCV000223798 ; RCV001175287
• dbSNP Id: rs876661359
• MyVariant Identifiers: chrMT:g.4315A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.4315A>G , J01415.2:m.4315A>G	GRCh38