Canonical Allele Identifier: CA913178938
Gene:

Linked Data

ClinVar Variation Id: 2583105
ClinVar RCV Id: RCV003334348
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8316T>C , J01415.2:m.8316T>C GRCh38
Search 100 bp 5'
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