Canonical Allele Identifier: CA913180446
Gene:

Linked Data

ClinVar Variation Id: 689987
ClinVar RCV Id: RCV000850845
dbSNP Id: rs1603220110

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5783G>A , J01415.2:m.5783G>A GRCh38