Canonical Allele Identifier: CA913178868
Gene:

Linked Data

ClinVar Variation Id: 690062
ClinVar RCV Id: RCV000850936
dbSNP Id: rs1603221389

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8298T>C , J01415.2:m.8298T>C GRCh38