Canonical Allele Identifier: CA913175296
Gene:

Linked Data

ClinVar Variation Id: 870596
ClinVar RCV Id: RCV001090167
dbSNP Id: rs2068750239
ERepo: CA913175296/MONDO:0044970/014
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15958A>T , J01415.2:m.15958A>T GRCh38
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