Canonical Allele Identifier: CA337100567
Gene:

Linked Data

ClinVar Variation Id: 690224
ClinVar RCV Id: RCV000851116
dbSNP Id: rs35788393
MyVariant Identifiers: chrMT:g.15904C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15904C>T , J01415.2:m.15904C>T GRCh38