Canonical Allele Identifier: CA913175137
Gene:

Linked Data

ClinVar Variation Id: 690218
ClinVar RCV Id: RCV000851110
dbSNP Id: rs1569484752
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15894G>A , J01415.2:m.15894G>A GRCh38
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