Canonical Allele Identifier: CA913169128
Gene:

Linked Data

ClinVar Variation Id: 689870
ClinVar RCV Id: RCV000850709
dbSNP Id: rs1603218872
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3288A>G , J01415.2:m.3288A>G GRCh38
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