Canonical Allele Identifier: CA254831

Gene:

Linked Data

• ClinVar Variation Id: 9556
• ClinVar RCV Id: RCV000010166 ; RCV000850777 ; RCV002291209
• dbSNP Id: rs199474673
• MyVariant Identifiers: chrMT:g.5521G>A (hg38)
• PubMed: PMID:9673981
• ERepo: CA254831/MONDO:0044970/014

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.5521G>A , J01415.2:m.5521G>A	GRCh38