Canonical Allele Identifier: CA913180169
Gene:

Linked Data

ClinVar Variation Id: 689971
ClinVar RCV Id: RCV000850828
dbSNP Id: rs1603220080

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5665A>G , J01415.2:m.5665A>G GRCh38