Canonical Allele Identifier: CA337096847

Gene:

Linked Data

• ClinVar Variation Id: 689877
• ClinVar RCV Id: RCV000850723
• dbSNP Id: rs193303033
• MyVariant Identifiers: chrMT:g.4312C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.4312C>T , J01415.2:m.4312C>T	GRCh38