Canonical Allele Identifier: CA913169046
Gene:

Linked Data

ClinVar Variation Id: 1684919
ClinVar RCV Id: RCV002248011
dbSNP Id: rs1603218861
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3264T>C , J01415.2:m.3264T>C GRCh38
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