Canonical Allele Identifier: CA913179058
Gene:

Linked Data

ClinVar Variation Id: 690081
ClinVar RCV Id: RCV000850956
dbSNP Id: rs1603221419

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8350A>G , J01415.2:m.8350A>G GRCh38