Canonical Allele Identifier: CA250414
Gene:

Linked Data

ClinVar Variation Id: 209213
ClinVar RCV Id: RCV000191152
MyVariant Identifiers: chrMT:g.5794_14876del (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5794_14876del , J01415.2:m.5794_14876del GRCh38