Canonical Allele Identifier: CA913180786
Gene:

Linked Data

ClinVar Variation Id: 690025
ClinVar RCV Id: RCV000850884
dbSNP Id: rs1603220167
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5889A>G , J01415.2:m.5889A>G GRCh38
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