Canonical Allele Identifier: CA913169592
Gene:

Linked Data

ClinVar Variation Id: 618221
ClinVar RCV Id: RCV000756363
dbSNP Id: rs1569484492
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12177A>G , J01415.2:m.12177A>G GRCh38
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