Canonical Allele Identifier: CA913180453
Gene:

Linked Data

ClinVar Variation Id: 689989
ClinVar RCV Id: RCV000850847
dbSNP Id: rs1603220117
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5786T>C , J01415.2:m.5786T>C GRCh38
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