Canonical Allele Identifier: CA915952146
Gene:

Linked Data

ClinVar Variation Id: 690194
ClinVar RCV Id: RCV000851082
dbSNP Id: rs1603223659
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12310dup , J01415.2:m.12310dup GRCh38
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