Canonical Allele Identifier: CA915952153
Gene:

Linked Data

ClinVar Variation Id: 690254
ClinVar RCV Id: RCV000851149
dbSNP Id: rs1603225607
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15944dup , J01415.2:m.15944dup GRCh38
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