Canonical Allele Identifier: CA913180524
Gene:

Linked Data

ClinVar Variation Id: 690000
ClinVar RCV Id: RCV000850858
dbSNP Id: rs1603220134
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5809G>A , J01415.2:m.5809G>A GRCh38
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