Canonical Allele Identifier: CA120562

Gene:

Linked Data

• ClinVar Variation Id: 9592
• ClinVar RCV Id: RCV000850713 ; RCV003162234 ; RCV004554594
• dbSNP Id: rs199474660
• MyVariant Identifiers: chrMT:g.3303C>T (hg38)
• ERepo: CA120562/MONDO:0044970/014
• PubMed: PMID:7906985 ; PMID:10431114

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.3303C>T , J01415.2:m.3303C>T	GRCh38