Canonical Allele Identifier: CA913178916
Gene:

Linked Data

ClinVar Variation Id: 690068
ClinVar RCV Id: RCV000850942
dbSNP Id: rs371589230
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8311T>A , J01415.2:m.8311T>A GRCh38
Search 100 bp 5'
Search 100 bp 3'