Canonical Allele Identifier: CA254830
Gene:

Linked Data

ClinVar Variation Id: 9552
ClinVar RCV Id: RCV000010161
dbSNP Id: rs118203893
MyVariant Identifiers: chrMT:g.5877C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5877C>T , J01415.2:m.5877C>T GRCh38