Canonical Allele Identifier: CA337100719
Gene:

Linked Data

ClinVar Variation Id: 1525977
ClinVar RCV Id: RCV002051604
dbSNP Id: rs371240719
MyVariant Identifiers: chrMT:g.16180_16181del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.16182_16183del , J01415.2:m.16182_16183del GRCh38
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