Canonical Allele Identifier: CA10581203
Gene:

Linked Data

ClinVar Variation Id: 235015
ClinVar RCV Id: RCV000223713 RCV000850730
dbSNP Id: rs876661361
MyVariant Identifiers: chrMT:g.4317del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4317del , J01415.2:m.4317del GRCh38
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