Canonical Allele Identifier: CA337097198
Gene:

Linked Data

ClinVar Variation Id: 689952
ClinVar RCV Id: RCV000850809
dbSNP Id: rs376884056
MyVariant Identifiers: chrMT:g.5601C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5601C>T , J01415.2:m.5601C>T GRCh38