Canonical Allele Identifier: CA913169035
Gene:

Linked Data

ClinVar Variation Id: 689862
ClinVar RCV Id: RCV000850699
dbSNP Id: rs1603218859

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3261A>G , J01415.2:m.3261A>G GRCh38