Canonical Allele Identifier: CA913179801
Gene:

Linked Data

ClinVar Variation Id: 689933
ClinVar RCV Id: RCV000850786
dbSNP Id: rs1603220014

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5540G>A , J01415.2:m.5540G>A GRCh38