Canonical Allele Identifier: CA913169088
Gene:

Linked Data

ClinVar Variation Id: 689867
ClinVar RCV Id: RCV000850705
dbSNP Id: rs1057516057

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3275C>A , J01415.2:m.3275C>A GRCh38