Canonical Allele Identifier: CA913178935
Gene:

Linked Data

ClinVar Variation Id: 690069
ClinVar RCV Id: RCV000850943
dbSNP Id: rs1603221400
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8315A>G , J01415.2:m.8315A>G GRCh38
Search 100 bp 5'
Search 100 bp 3'