Canonical Allele Identifier: CA913177281
Gene:

Linked Data

ClinVar Variation Id: 690035
ClinVar RCV Id: RCV000850908
dbSNP Id: rs1603220992

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.7518A>G , J01415.2:m.7518A>G GRCh38