Canonical Allele Identifier: CA913179051
Gene:

Linked Data

ClinVar Variation Id: 690078
ClinVar RCV Id: RCV000850953
dbSNP Id: rs1603221417

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8347A>G , J01415.2:m.8347A>G GRCh38