Canonical Allele Identifier: CA913179884
Gene:

Linked Data

ClinVar Variation Id: 689944
ClinVar RCV Id: RCV000850800
dbSNP Id: rs1603220029

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5566A>G , J01415.2:m.5566A>G GRCh38