Canonical Allele Identifier: CA913177697
Gene:

Linked Data

ClinVar Variation Id: 689879
ClinVar RCV Id: RCV000850725
dbSNP Id: rs1603219401
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4314T>C , J01415.2:m.4314T>C GRCh38
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