Canonical Allele Identifier: CA915952210
Gene:

Linked Data

ClinVar Variation Id: 689990
ClinVar RCV Id: RCV000850848
dbSNP Id: rs1603220115

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5786dup , J01415.2:m.5786dup GRCh38