Canonical Allele Identifier: CA128830

Gene:

Linked Data

• ClinVar Variation Id: 30003
• ClinVar RCV Id: RCV000022898
• dbSNP Id: rs387906421
• MyVariant Identifiers: chrMT:g.14674T>G (hg38)
• PubMed: PMID:21194154

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.14674T>G , J01415.2:m.14674T>G	GRCh38