Canonical Allele Identifier: CA337100622

Gene:

Linked Data

• ClinVar Variation Id: 690265
• ClinVar RCV Id: RCV000851163
• dbSNP Id: rs201041059
• MyVariant Identifiers: chrMT:g.15978C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.15978C>T , J01415.2:m.15978C>T	GRCh38