Canonical Allele Identifier: CA913179106
Gene:

Linked Data

ClinVar Variation Id: 690085
ClinVar RCV Id: RCV000850962
dbSNP Id: rs1603221428

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8364A>T , J01415.2:m.8364A>T GRCh38