Canonical Allele Identifier: CA131018
Gene:

Linked Data

ClinVar Variation Id: 42233
ClinVar RCV Id: RCV000035058
dbSNP Id: rs111033185
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.958_960dup , J01415.2:m.958_960dup GRCh38
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