Canonical Allele Identifier: CA913177287
Gene:

Linked Data

ClinVar Variation Id: 690036
ClinVar RCV Id: RCV000850909
dbSNP Id: rs1603220993

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.7520G>A , J01415.2:m.7520G>A GRCh38