Canonical Allele Identifier: CA915952206
Gene:

Linked Data

ClinVar Variation Id: 689929
ClinVar RCV Id: RCV000850782
dbSNP Id: rs1603220010

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5536_5537insT , J01415.2:m.5536_5537insT GRCh38