Canonical Allele Identifier: CA913178984
Gene:

Linked Data

ClinVar Variation Id: 1684916
ClinVar RCV Id: RCV002248008
dbSNP Id: rs2124594549

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8328G>A , J01415.2:m.8328G>A GRCh38