Canonical Allele Identifier: CA913169731
Gene:

Linked Data

ClinVar Variation Id: 690158
ClinVar RCV Id: RCV000851043
dbSNP Id: rs1603223616

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12213G>A , J01415.2:m.12213G>A GRCh38