Canonical Allele Identifier: CA913169627
Gene:

Linked Data

ClinVar Variation Id: 1684914
ClinVar RCV Id: RCV002248006
dbSNP Id: rs2068730503
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12187C>A , J01415.2:m.12187C>A GRCh38
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