Canonical Allele Identifier: CA337100595
Gene:

Linked Data

ClinVar Variation Id: 690249
ClinVar RCV Id: RCV000851143
dbSNP Id: rs878981265
MyVariant Identifiers: chrMT:g.15939C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15939C>T , J01415.2:m.15939C>T GRCh38