Canonical Allele Identifier: CA913180507
Gene:

Linked Data

ClinVar Variation Id: 689996
ClinVar RCV Id: RCV000850854
dbSNP Id: rs1603220128
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5802T>C , J01415.2:m.5802T>C GRCh38
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