Canonical Allele Identifier: CA337096869
Gene:

Linked Data

ClinVar Variation Id: 689901
ClinVar RCV Id: RCV000850752
dbSNP Id: rs386828941
MyVariant Identifiers: chrMT:g.4385A>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4385A>T , J01415.2:m.4385A>T GRCh38