Canonical Allele Identifier: CA913179040
Gene:

Linked Data

ClinVar Variation Id: 690075
ClinVar RCV Id: RCV000850949
dbSNP Id: rs1603221411

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8343A>G , J01415.2:m.8343A>G GRCh38