Canonical Allele Identifier: CA345919
Gene:

Linked Data

ClinVar Variation Id: 155890
ClinVar RCV Id: RCV000144021
dbSNP Id: rs587776441
MyVariant Identifiers: chrMT:g.1644G>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.1644G>T , J01415.2:m.1644G>T GRCh38