Canonical Allele Identifier: CA337096856

Gene:

Linked Data

• ClinVar Variation Id: 689886
• ClinVar RCV Id: RCV000850735
• dbSNP Id: rs878959563
• MyVariant Identifiers: chrMT:g.4335C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.4335C>T , J01415.2:m.4335C>T	GRCh38