Canonical Allele Identifier: CA337100608

Gene:

Linked Data

• ClinVar Variation Id: 690256
• ClinVar RCV Id: RCV000851151
• dbSNP Id: rs202014122
• MyVariant Identifiers: chrMT:g.15946C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.15946C>T , J01415.2:m.15946C>T	GRCh38