Canonical Allele Identifier: CA913175179
Gene:

Linked Data

ClinVar Variation Id: 690230
ClinVar RCV Id: RCV000851122
dbSNP Id: rs1603225583
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15911A>G , J01415.2:m.15911A>G GRCh38
Search 100 bp 5'
Search 100 bp 3'