Canonical Allele Identifier: CA337096881
Gene:

Linked Data

ClinVar Variation Id: 689918
ClinVar RCV Id: RCV000850770
dbSNP Id: rs878986264
MyVariant Identifiers: chrMT:g.4455A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4455A>G , J01415.2:m.4455A>G GRCh38