Canonical Allele Identifier: CA130992

Gene:

Linked Data

• ClinVar Variation Id: 42205
• ClinVar RCV Id: RCV000035029
• dbSNP Id: rs28358571
• MyVariant Identifiers: chrMT:g.1189T>C (hg38)
• PubMed: PMID:9461455 ; PMID:11406419

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.1189T>C , J01415.2:m.1189T>C	GRCh38