Canonical Allele Identifier: CA10581202

Gene:

Linked Data

• ClinVar Variation Id: 235014
• ClinVar RCV Id: RCV000223881 ; RCV000850728
• dbSNP Id: rs876661360
• MyVariant Identifiers: chrMT:g.4316A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.4316A>G , J01415.2:m.4316A>G	GRCh38