Canonical Allele Identifier: CA913180112
Gene:

Linked Data

ClinVar Variation Id: 689964
ClinVar RCV Id: RCV000850821
dbSNP Id: rs1603220068

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5645G>A , J01415.2:m.5645G>A GRCh38