Canonical Allele Identifier: CA658799934

Gene:

Linked Data

• ClinVar Variation Id: 505197
• ClinVar RCV Id: RCV000601445
• dbSNP Id: rs1556422517
• MyVariant Identifiers: chrMT:g.1290C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.1290C>T , J01415.2:m.1290C>T	GRCh38