Canonical Allele Identifier: CA913180290
Gene:

Linked Data

ClinVar Variation Id: 812543
ClinVar RCV Id: RCV001003371
dbSNP Id: rs1603220093

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5702A>G , J01415.2:m.5702A>G GRCh38