Canonical Allele Identifier: CA128833
Gene:

Linked Data

ClinVar Variation Id: 30007
ClinVar RCV Id: RCV000022907
dbSNP Id: rs387906736
MyVariant Identifiers: chrMT:g.5556G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5556G>A , J01415.2:m.5556G>A GRCh38