Canonical Allele Identifier: CA915952076
Gene:

Linked Data

ClinVar Variation Id: 689815
ClinVar RCV Id: RCV000850641
dbSNP Id: rs1603218455
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.597_598insT , J01415.2:m.597_598insT GRCh38
Search 100 bp 5'
Search 100 bp 3'