Canonical Allele Identifier: CA913179043
Gene:

Linked Data

ClinVar Variation Id: 690076
ClinVar RCV Id: RCV000850951
dbSNP Id: rs1603221413

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8345C>T , J01415.2:m.8345C>T GRCh38