Canonical Allele Identifier: CA10581310

Gene:

Linked Data

• ClinVar Variation Id: 235438
• ClinVar RCV Id: RCV000224569 ; RCV000850756
• dbSNP Id: rs375986475
• MyVariant Identifiers: chrMT:g.4388A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.4388A>G , J01415.2:m.4388A>G	GRCh38