Canonical Allele Identifier: CA913179093
Gene:

Linked Data

ClinVar Variation Id: 690083
ClinVar RCV Id: RCV000850959
dbSNP Id: rs1603221422

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8360A>G , J01415.2:m.8360A>G GRCh38