Canonical Allele Identifier: CA913175199
Gene:

Linked Data

ClinVar Variation Id: 972986
ClinVar RCV Id: RCV001249307
dbSNP Id: rs2068749891
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15917C>T , J01415.2:m.15917C>T GRCh38
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