Canonical Allele Identifier: CA913179941
Gene:

Linked Data

ClinVar Variation Id: 689950
ClinVar RCV Id: RCV000850807
dbSNP Id: rs1603220042

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5592A>G , J01415.2:m.5592A>G GRCh38