Canonical Allele Identifier: CA913180026
Gene:

Linked Data

ClinVar Variation Id: 689960
ClinVar RCV Id: RCV000850817
dbSNP Id: rs1603220062

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5619G>A , J01415.2:m.5619G>A GRCh38