Canonical Allele Identifier: CA130999

Gene:

Linked Data

• ClinVar Variation Id: 42213
• ClinVar RCV Id: RCV000035038
• dbSNP Id: rs111033354
• MyVariant Identifiers: chrMT:g.1310C>T (hg38)
• PubMed: PMID:2025303 ; PMID:7723627 ; PMID:9519725

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.1310C>T , J01415.2:m.1310C>T	GRCh38