Canonical Allele Identifier: CA913179904
Gene:

Linked Data

ClinVar Variation Id: 689947
ClinVar RCV Id: RCV000850803
dbSNP Id: rs1603220033

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5573A>G , J01415.2:m.5573A>G GRCh38