Canonical Allele Identifier: CA120553

Gene:

Linked Data

• ClinVar Variation Id: 9577
• ClinVar RCV Id: RCV000010190
• dbSNP Id: rs387906420
• MyVariant Identifiers: chrMT:g.616T>G (hg38)
• PubMed: PMID:20142618

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.616T>G , J01415.2:m.616T>G	GRCh38