Canonical Allele Identifier: CA913180297
Gene:

Linked Data

ClinVar Variation Id: 689977
ClinVar RCV Id: RCV000850834
dbSNP Id: rs1556423024

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5705A>G , J01415.2:m.5705A>G GRCh38