Canonical Allele Identifier: CA913175725
Gene:

Linked Data

ClinVar Variation Id: 689832
ClinVar RCV Id: RCV000850659
dbSNP Id: rs1569483788
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.647A>G , J01415.2:m.647A>G GRCh38
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