Canonical Allele Identifier: CA254830

Gene:

Linked Data

• ClinVar Variation Id: 9552
• ClinVar RCV Id: RCV000010161
• dbSNP Id: rs118203893
• MyVariant Identifiers: chrMT:g.5877C>T (hg38)
• PubMed: PMID:11594340

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.5877C>T , J01415.2:m.5877C>T	GRCh38