Canonical Allele Identifier: CA913178873
Gene:

Linked Data

ClinVar Variation Id: 690063
ClinVar RCV Id: RCV000850937
dbSNP Id: rs1603221391
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8299G>A , J01415.2:m.8299G>A GRCh38
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