Canonical Allele Identifier: CA254842

Gene:

Linked Data

• ClinVar Variation Id: 9606
• ClinVar RCV Id: RCV000010229 ; RCV001251031 ; RCV002247293 ; RCV002291210
• dbSNP Id: rs121434470
• MyVariant Identifiers: chrMT:g.4300A>G (hg38)
• PubMed: PMID:12767666
• ERepo: CA254842/MONDO:0044970/014

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.4300A>G , J01415.2:m.4300A>G	GRCh38